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¿Tienes experiencia en el sector óptico y quieres progresar en tu carrera profesional en una empresa que comparte tus inquietudes? En Opticalia buscamos el talento de personas como tú, profesionales que entienden el mundo de la óptica de manera fresca e innovadora. Personas que piensan en el cliente, que saben conectar emocionalmente con la gente y que harán todo lo posible para que en nuestras ópticas se viva una experiencia única. Todos nuestros compañeros y compañeras cuentan con una alta cualificación ya que ofrecemos la posibilidad de estar en formación permanente gracias a nuestro campus. ¿Qué buscamos? Actualmente necesitamos incorporar dos profesionales en las posiciones de Óptico/a y Audioprotesista. ¿Cuáles serían tus funciones? Como optometrista : Revisión y ajustes de graduación. Adaptar lentes de contacto. Montaje de gafas en taller. Atención y venta al paciente/cliente. Como audioprotesista: Revisión y exámenes auditivos Ajustes y adaptación de audífonos Atención y venta al paciente/cliente. ¿Qué ofrecemos? Contrato Indefinido. Jornada completa en turno partido de lunes a viernes y sábados por la mañana. Desarrollo profesional en empresa líder en el sector. Acceso a un programa de formación continua para seguir adquiriendo conocimientos técnicos y competencias para desarrollar el trabajo de manera eficaz. Excelente ambiente de trabajo. Si crees que cumples con los requisitos y quieres formar parte del equipo de Opticalia, no dudes en inscribirte. Te esperamos :)

We are building a new team of Medical Science Liaisons (MSLs) across Europe and are looking for an MSL for Spain and Italy. This key field-based role involves establishing and nurturing relationships with Principal Investigators (PIs), Key Opinion Leaders (KOLs), and other stakeholders. The MSL will engage in scientific discussions, build robust networks, educate on disease and screening processes, and raise awareness about clinical trials, particularly focusing on viral hepatitis. A crucial part of this role is to support patient recruitment for clinical trials. Key Responsibilities: • Educate healthcare professionals (HCPs) on liver disease, specifically viral hepatitis, focusing on treatment and diagnosis through scientific exchange., • Present the latest clinical data and scientific information to HCPs through peer-to-peer interactions., • Develop an understanding of regional/local healthcare systems, treatment patterns, and KOLs in viral hepatitis., • Facilitate medical and scientific field intelligence by maintaining a list of investigators and their networks, and understanding competitor research activities., • Promote awareness of clinical trials to enhance patient recruitment and facilitate effective patient screening., • Lead the development and execution of medical regional territory plans., • Collaborate with Clinical Trial Leads, Clinical Research Associates (CRAs), and other stakeholders in clinical research trials., • Attend medical congresses to build relationships, advocate, and present key data., • Collaborate with internal stakeholders by sharing relevant insights and contributing to scientific knowledge development., • Ensure compliance with local/regional guidelines related to scientific communication and regulatory environments., • Advanced clinical/medical degree (Pharm D, MD, PhD) from an accredited institution; a master's degree is preferred., • Prior Medical Science Liaison (MSL) or Clinical Trial Educator (CTE) experience is required., • Clinical trial experience is preferred., • Minimum of 1-year experience in hepatology and/or infectious diseases (excluding vaccination) is highly preferred., • Demonstrated expertise in discussing scientific content with multiple audiences., • Knowledge of local and regional guidelines related to compliant scientific communication and regulatory environments., • Proficiency with support technology (PC and CRM tools, Microsoft Teams, SharePoint, PowerPoint, Outlook)., • Ability to travel up to 70% of the time., • Valid driver’s license required., • Excellent written and oral communication skills. LI-CES #LI-CS1 IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide. Learn more at (website). At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We foster a culture of belonging by valuing diverse perspectives and providing opportunities for all talented employees worldwide. When our employees bring their authentic selves and diverse experiences to work, we enable extraordinary achievements. Multifaceted thought processes spark innovation, and multi-talented collaboration harnesses this innovation for superior outcomes. Key Skills: Presentation Skills, Time Management, Clinical Research, Communication Skills, GCP, Infusion Experience, Managed Care, Hospice Care, Conflict Management, Clinical Trials, Research Experience, Home Care Employment Type: Full-Time Experience: Years Vacancy: 1 #J-18808-Ljbffr

Dentists wanted to work in private dental clinics in Ireland. We are currently looking for Dentists to work in private clinics in Ireland, specializing in: • General Dentistry, • Degree in Dentistry from an EU University, • Fluent English (C1), • Around €100K per annum gross for general dentists, • Relocation package, • Assistance with registration as a dentist in the Republic of Ireland #J-18808-Ljbffr

TFS HealthScience is seeking a highly strategic and experienced Medical Director with expertise in Internal Medicine or Neuroscience to drive clinical development excellence and support business growth. This role is pivotal in shaping study design, leading bid defenses, and ensuring medical oversight across key projects. As a Medical Director, you will serve as a trusted scientific partner, engaging with clients, guiding protocol development, and providing medical monitoring when required. If you are a clinically grounded leader with a strong commercial mindset and a passion for advancing drug development, we invite you to join our global team. Key Responsibilities : • Strategic Leadership : Act as a key scientific advisor in bid defense meetings (BDM), RFP responses, and proposal development, ensuring compelling and medically sound strategies., • Study Design & Protocol Development : Provide expert input on trial design, patient recruitment, and regulatory strategy to optimize study success., • Medical Oversight : Lead medical monitoring activities across assigned projects and step in as a hands-on medical monitor when needed., • Scientific Advocacy : Represent TFS at client meetings, industry conferences, and scientific events, reinforcing our reputation as a trusted CRO partner., • Board-certified in Internal Medicine or Neuroscience., • Deep knowledge of GCP, ICH guidelines, and regulatory requirements (FDA / EMA)., • Business acumen : Proven ability to support business development with a strategic, client-focused approach., • Exceptional communicator : Strong presentation, negotiation, and interpersonal skills for engaging stakeholders at all levels. Our journey began over 25 years ago in Sweden, in the city of Lund. As a global CRO with the ultimate goal of ensuring patients’ safety and well-being, we provide biotechnology and pharmaceutical companies with tailored clinical development solutions. We currently operate in 17 countries across Europe, North America, Asia Pacific and the Middle East. Our core values of Trust, Quality, Flexibility and Passion are what make TFS Healthscience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organization. #J-18808-Ljbffr

Organisation/Company Autonomous University of Madrid (Universidad Autónoma de Madrid) Department Teaching and Research Staff (Personal Docente e Investigador) Research Field Physics Researcher Profile First Stage Researcher (R1) Positions Master Positions Country Spain Application Deadline 8 Sep 2025 - 00:00 (Europe/Madrid) Type of Contract Permanent Job Status Full-time Hours Per Week 37,5 Offer Starting Date 1 Oct 2025 Is the job funded through the EU Research Framework Programme? Not funded by a EU programme Reference Number TEC-2024/TEC-380 Is the Job related to staff position within a Research Infrastructure? No Predoctoral contract in a low temperature and high magnetic field laboratory Scanning Tunneling Microscopy experiments in magnetic materials. Synthesis of single crystals of magnetic materials. Experience in Scanning Tunneling Microscopy at low temperatures (liquid Helium) and in cryogenics. Experience in studying magnetic systems. Experience in single crystal synthesis Specific Requirements Knowledge of cryogenics and operation of superconducting coils Languages ENGLISH Level Excellent Languages SPANISH Level Excellent 1929 €/monthly gross salary Eligibility criteria Undergraduate marks and previous experience in the research themes of the position Selection process Commission of senior members of the Department. Additional comments Expected end of contract: 31/08/2026 Applications to this offer must compulsory be registered through the online application system of UAM. Nevertheless, prospective applicants are encouraged to contact the PI beforehand to discuss their suitability for the position, and to seek for assistance with the online application system . #J-18808-Ljbffr

Buscamos un / a docente-investigador / a para incorporarseen nuestra institución educativa. La persona seleccionada deberá contar con un sexenio de investigación reconocido en Educación y / o Tecnología Educativa y asumirá un papel transversal en la impartición de asignaturas en diferentes titulaciones, según su perfil académico y profesional. Detalles del Puesto : Docencia interdisciplinar adaptada a las necesidades académicas de diversas titulaciones. • Enviar o adjuntar el reconocimiento oficial de sexenio de investigación en Educación y / o Tecnología Educativa(imprescindible)., • Experiencia en docencia universitaria y capacidad para adaptarse a diversos programas de estudios., • Incorporación a un equipo docente dinámico y comprometido con la excelencia educativa. Con En • Madrid, Comunidad de Madrid, España #J-18808-Ljbffr

About Us Based in Barcelona and Treviso, INDIBA Group stands at the forefront of global leadership in Aesthetics, Beauty, Rehabilitation, Sports, Intimate Health, Pharma, and Animal Health solutions, with a rich 40-year history of scientific innovation. Our cutting-edge 448 kHz frequency technology is the cornerstone of our therapies, empowering individuals to enhance their lives and recover from injuries across various sectors. With the integration of K-LASER, a global leader in medical lasers, we are committed to advancing treatments, embracing new technologies, and expanding our global presence in medical research. Our mission is revitalizing lives, and our teams work daily towards this goal. We seek a senior leader to oversee the Medical Affairs & Training Department. This strategic role combines regulatory and clinical responsibilities with scientific communication and training leadership. The ideal candidate will have deep medical expertise, stakeholder engagement skills, and the ability to translate clinical insights into business value while supporting our company positioning. • Lead the development and strategic use of clinical evidence to support product registration and ensure compliance with global medical device regulations., • Oversee the preparation of clinical documentation, including trial protocols, regulatory submissions, and reports to health authorities and notified bodies., • Supervise clinical trials and post-market surveillance, maintaining relationships with key opinion leaders and investigators., • Represent the medical department in audits, inspections, and quality reviews requiring scientific expertise., • Provide scientific support and strategic guidance to internal departments such as Commercial, Marketing, R&D, Regulatory, and Quality., • Guide the development of scientific materials, publications, and conference contributions to enhance our position in the medical community., • Lead the Training team to deliver high-quality programs aligned with clinical data, product claims, and corporate goals., • Monitor emerging clinical trends and innovations to inform product development and positioning., • Ensure the effectiveness of the medical vigilance system in collaboration with relevant departments., • Minimum of 10 years’ experience in Pharmaceutical, Medical Devices, or regulatory consultancy sectors, in areas such as Medical/Scientific Department, Clinical Research, Medical Writing, or Scientific Marketing., • Experience in writing clinical reports (expert reports, review reports, clinical/pharmacological/pharmacovigilance studies, phase III/IV studies)., • Degree in Health Sciences (Medicine, Pharmacy, Human Biology, or Biomedical Science); postgraduate studies in Pharmaceutical, Cosmetic, or Aesthetic/Rehabilitation Medicine are a plus., • Strong knowledge of clinical research methodology., • Fluent in Spanish and English, both verbal and written; additional languages are a plus., • Full-time, permanent contract., • Location: Sant Cugat del Vallés., • Hybrid work model., • Attractive remuneration package and fringe benefits., • Multinational, flexible environment. #J-18808-Ljbffr

Wanting to make a true difference by setting the strategy and leading the Rare Diseases Medical team of Nordisk Spain? Do you have the expertise to lead and inspire a team towards scientific excellence? We are seeking a Head of Medical Affairs Rare Disease to join our team in Madrid, Spain. Read on and apply today for a life-changing career. Novo Nordisk's pipeline in rare diseases spans several therapeutic areas including rare blood disorders and rare endocrine disorders. We have new treatments for new areas on the horizon, always with the same purpose: advancing treatments that address the unique challenges faced by individuals with these conditions, aiming to improve diagnosis, treatment, and overall management of rare diseases. As a Head of Medical Affairs Rare Disease , you will drive the medical strategy and lead the plan of an exciting pipeline, directly and through the management of the team. • Be a true leader: foster the team to take ownership and act boldly, coach and share feedback, understand and identify training needs, ensure team wellbeing and motivation., • Defining the KOL engagement strategy: building and growing a solid scientific relationship with appropriate physicians, scientific societies, and other relevant stakeholders., • Provide cross-functional expertise: to internal and external stakeholders, and represent Novo Nordisk Spain at local and global meetings., • Ensure accuracy of medical and scientific information: regarding Novo Nordisk products through all channels, working according to Business Ethics procedures, local law, NNWay, and NN policies & guidelines., • Education: Medical Doctor, • Solid experience and a proven track record in the pharmaceutical industry from the Medical Affairs area, with at least 5 years in a leadership role driving medical strategy and leading both functional and cross-functional teams., • Experience across a wide range of therapeutic areas, demonstrating adaptability and learning ability. Experience in Rare Diseases is required, ideally in Hemophilia or Endocrine disorders. In this role, you will report to the VP of Clinical Medical & Regulatory, working closely with the RareD BU Senior Director. The CMR department includes passionate colleagues leading the development of medicines, bringing them to patients, and driving change in disease areas by focusing on improving outcomes and reducing health inequalities. We are a proud life sciences company. Life is our reason to exist. We are inspired by life in all its forms and challenges. For our employees, life encompasses groundbreaking scientific research and our personal lives that motivate us to perform our best. Ultimately, life is why we are here: to ensure people can lead a life independent of chronic disease. Apply before 24th April 2025. Please note that, due to Data Privacy Policy, we cannot accept CVs and applications sent via email or other channels outside our Application System. We are committed to an inclusive recruitment process and equal opportunity for all applicants. At Novo Nordisk, we recognize that it is no longer enough to aspire to be the best company in the world; we need to be the best company for the world. This is only possible with talented employees from diverse backgrounds and cultures. We are committed to creating an inclusive culture that celebrates diversity among our employees, the patients we serve, and the communities we operate in. Together, we're life-changing. #J-18808-Ljbffr

Universidad Camilo José Cela Buscamos un/a docente-investigador/a para incorporarse en nuestra institución educativa. La persona seleccionada deberá contar con un sexenio de investigación reconocido en Geografía y asumirá un papel transversal en la impartición de asignaturas en diferentes titulaciones, según su perfil académico y profesional. Docencia interdisciplinar adaptada a las necesidades académicas de diversas titulaciones. • Enviar o adjuntar el reconocimiento oficial de sexenio de investigación en Geografía (imprescindible)., • Experiencia en docencia universitaria y capacidad para adaptarse a diversos programas de estudios., • Incorporación a un equipo docente dinámico y comprometido con la excelencia educativa., • Oportunidad de contribuir al desarrollo académico en un entorno innovador y colaborativo. #J-18808-Ljbffr

Every 30 minutes, a stroke patient who could have been saved either dies or is permanently disabled because they were treated in the wrong hospital. Our mission is clear: to increase the number of patients treated in stroke-ready hospitals and to optimize the quality of treatment in all existing stroke centers. We are building a global community of stroke centers and stroke-ready hospitals, working tirelessly to improve the quality of treatment for every stroke patient. This is a unique opportunity to join IQVIA to enhance stroke care worldwide through a corporate social responsibility project. To help lead this change, we’re looking for a passionate Consultants to join our team in Central Spain. Responsibilities: After comprehensive and ongoing training, you will be ready to: • Enhance the efficiency of stroke patient management, • Support hospitals and healthcare professionals with continuous training and organizational tools, • Serve as an expert Therapeutic Consultant, promoting new diagnostic and treatment guidelines to hospitals, • Foster and promote quality monitoring programs to ensure consistent hospital performance, • Expand the project's reach to new hospitals, • Lead multidisciplinary stroke teams through continuous improvement, • Excellent scientific background, ideally with a PhD in Neuroscience, • High motivation and strong interpersonal skills, • Fluency in English and Spanish, • Leadership abilities, • Proactive, flexible, and strong problem-solving skills, • Availability to travel up to 70% of the time, • Eligibility to work full-time #LI-CES #LI-VK1 IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at . At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. #J-18808-Ljbffr

En HM Hospitales tenemos el objetivo de prestar la mejor calidad asistencial a pacientes y familiares. No sólo eso, también estamos involucrados e involucradas en la docencia y la investigación. Todo ello, en constante innovación tecnológica. Somos un Grupo comprometido con la igualdad de oportunidades, la diversidad y la inclusión. Apostamos por ti, por el talento, por la vocación…por ello, nuestros procesos de selección están libres de cualquier tipo de discriminación. Actualmente, formamos un equipo de más de 6.000 profesionales, presentes en 50 centros (22 Hospitales, 3 Centros Integrales, 3 centros especializados y 22 Policlínicos) siendo así el Grupo Hospitalario privado de referencia en la Comunidad de Madrid, Galicia, León, Barcelona y Málaga ¡Queremos que formes parte de nuestro Equipo! ¿En qué centro HM Hospitales te gustaría seguir desarrollándote? ¿Cuentas con experiencia en Electrofisiología y quieres unirte a HM Hospitales? Si la respuesta es SÍ, ¡¡sigue leyendo!! Nos gustaría contar contigo en el equipo de enfermería de la unidad de electrofisiología para nuestro hospital HM Monteprincipe, ubicado en Boadilla del Monte. Echa un vistazo a las condiciones del puesto: • Hospital: HM Monteprincipe (Boadilla del Monte), • Unidad: Electrofisiología, • Turno: tarde (de 15:00 a 22:00 horas) Lunes a viernes, • Jornada: completa, • Contrato: interinidad de larga duración., • Tendrás que tener finalizada la Diplomatura y/o Grado en Enfermería, y estar colegiado/a., • Será importante que tengas disponibilidad para trabajar en la zona de Boadilla del Monte., • Experiencia en electrofisiología, cardiología. #J-18808-Ljbffr

Social network you want to login/join with: col-narrow-left Madrigal Pharmaceuticals madrid, Spain Other - Yes col-narrow-right 535361532931656908832460 2 23.07.2025 06.09.2025 col-wide The Company Madrigal is a biopharmaceutical company pursuing novel therapeutics for nonalcoholic steatohepatitis (NASH), also known as metabolic dysfunction associated steatohepatitis (MASH). NASH is a growing global health burden in all regions of the world, but many patients with NASH remain undiagnosed. Madrigal’s novel therapeutic emerged from a research program examining the role of the thyroid hormone receptor (THR) β pathway in liver health. Madrigal scientists and researchers, working with leading experts in hepatology, have been studying the therapy’s ability to target the underlying causes of NASH by reducing or eliminating liver fat (steatosis) as well as reducing liver inflammation, liver cell ballooning (hepatocyte cell death), and liver fibrosis that can lead to cirrhosis. Madrigal’s lead candidate, Rezdiffra (resmetirom), is a once-daily, oral, liver-directed thyroid hormone receptor-β (THR-β) agonist designed to target key underlying causes of NASH. There have been no prior treatments available to halt or improve fibrosis, thus resolving NASH. Based on Phase 3 results reported to date, the U.S. FDA granted accelerated approval for their therapy for the treatment of adults with NASH with moderate to advanced liver fibrosis (consistent with stages F2 to F3 fibrosis). Madrigal is currently conducting multiple Phase 3 clinical trials to evaluate the safety and efficacy of resmetirom for the treatment of NASH, including the pivotal MAESTRO-NASH biopsy study in patients with significant fibrosis, the MAESTRO-NASH Outcomes study in patients with NASH with compensated cirrhosis and the MAESTRO-NAFLD-1 safety study. Positive results from the pivotal MAESTRO-NASH biopsy study were published in the New England Journal of Medicine in February 2024. The company announced recent new data from the Phase 3 MAESTRO-NASH Study of Rezdiffra presented at the EASL Congress on June 6th, 2024. The key takeaways included: • Late-breaking AI-based analysis of MAESTRO-NASH biopsy data demonstrates Rezdiffra improved key fibrotic features that are predictive of progression to decompensated cirrhosis., • Noninvasive test data through three years of treatment demonstrates durable treatment response to Rezdiffra; 91% of patients achieved improvement or stabilization of liver stiffness., • First analysis of health-related quality of life data from MAESTRO-NASH demonstrates Rezdiffra improved patient worry, health distress and stigma. Rezdiffra is Madrigals’ only drug that has been approved for sale and it has been approved only for the treatment of adults with noncirrhotic NASH with moderate to advanced liver fibrosis in the United States. The company is focusing a significant portion of their activities and resources on Rezdiffra, and they believe their prospects are highly dependent on, and a significant portion of the value of the company relates to, the ability to successfully commercialize Rezdiffra for the treatment of adults with NASH with moderate to advanced liver fibrosis in the United States and beyond. NASH / MASH NASH is a leading cause of liver related mortality and an increasing burden on healthcare systems globally. Additionally, patients with NASH, especially those with more advanced metabolic risk factors (hypertension, concomitant type 2 diabetes), are at increased risk for adverse cardiovascular events and increased morbidity and mortality. Once NASH progresses to significant liver fibrosis (consistent with F2/F3) the risk of adverse liver outcomes increases dramatically: • The risk of liver-related mortality and other liver-related events (e.g. transplant) increases meaningfully in patients with increasing degrees of liver fibrosis. Patients with significant liver fibrosis have an approximately 10-17X increased risk of liver-related mortality versus patients without liver fibrosis., • NASH is rapidly becoming the leading cause of liver transplantation in the U.S. Bill Sibold, Madrigal CEO, recently highlighted “Madrigal is the first company to deliver an approved therapy for patients with NASH, which we believe will give us a strong competitive advantage for many years to come. As a once-daily, well-tolerated, liver-directed, oral medicine that has demonstrated unprecedented efficacy in a pivotal Phase 3 trial, Rezdiffra is well positioned to become the foundational therapy for this serious disease.” He continued, “We are focused on executing this first-in-disease launch, where our expert team is partnering with the NASH community to establish treatment pathways for patients, laying the groundwork for our long term leadership”. Purpose of the Position • The Senior Director Medical Affairs, Spain is the Senior Medical Leader for Madrigal Pharmaceuticals in Spain, overseeing all aspects of the Medical Affairs and acting as the primary contact for Medical Affairs in the country., • Key responsibilities include developing and executing the Medical Affairs strategy tailored for Spain, ensuring a compliant and high-performing Medical Affairs organization and successful launch of resmetirom., • The role involves representing local needs and opportunities within regional and global contexts, serving on Spain's Leadership Team, and representing Madrigal Pharmaceuticals in external engagements requiring the presence of the Spain’s Senior Medical Leader. Develops and Executes Medical Affairs Strategy: • Strategically develops and executes Medical Affairs (MA) plans, ensuring alignment with local needs and global strategies., • Act as the primary external interface with stakeholders including insurers, government leaders, professional societies, and medical-scientific institutions., • Leads and executes medical research and implementation strategies for Madrigal Pharmaceuticals' products., • Partners with Global Medical Affairs, Market Access, and Commercial teams to engage payers, policymakers, and decision-makers in support of Madrigal's products., • Builds and maintains relationships with scientific leaders relevant to current and future needs., • Gathers local insights from healthcare providers (HCPs) and patients to inform regional and global strategies., • Provides oversight to Spain’s Medical Team (Medical Science Liaisons/Medical Advisors), ensuring robust and compliant activities supporting scientific exchange., • Manages Compassionate Use Requests, patient access programs, and similar initiatives., • Provides medical expertise to commercial product teams to enhance scientific and medical value. Experience and Professional Qualifications Minimum: • A minimum of 5-10 years of global biopharmaceutical industry experience in clinical development and/or medical affairs with demonstrated track record of success., • A minimum of 3-5 years of people-management experience in pharmaceutical industry., • Demonstrated organizational skills, including ability to set goals and align priorities., • Additional advanced degrees, entry on a specialist register (pharmaceutical medicine or a relevant clinical specialty) and a current ‘license to practice’ are a strong plus., • Specialty clinical training (i.e., a residency +/- fellowship), • Over 10 years of experience in medical affairs #J-18808-Ljbffr

Join to apply for the Freelance Senior / Medical Director (Neurology - Bid Defense Support) role at TFS HealthScience 3 weeks ago Be among the first 25 applicants Join to apply for the Freelance Senior / Medical Director (Neurology - Bid Defense Support) role at TFS HealthScience Get AI-powered advice on this job and more exclusive features. TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Freelance Senior / Medical Director (Neurology - Bid Defense Support). About this role TFS HealthScience isseeking a highly flexible board-certified Neurology specialist to support upcoming Bid Defense Meetings. This freelance role involves contributing expert input during proposal preparation (e.g. protocol review) and participating in the Bid Defense Meeting itself. Ideally, the successful candidate would also be available for medical monitoring support if the project is awarded — although this is not a requirement. This is a strategic role where your expertise will be key to demonstrating credibility and depth of knowledge to potential sponsors. We are looking for someone confident, articulate, and experienced enough to engage with clients at a high level and reinforce the strength of our clinical team. This role is pivotal in shaping study design, leading bid defenses and ensuring medical oversight across key projects. If you are a clinically grounded leader with a strong commercial mindset and a passion for advancing drug development, we invite you to join our global team. Key Responsibilities • Strategic Leadership: Act as a key scientific advisor in bid defense meetings (BDM), RFP responses, and proposal development, ensuring compelling and medically sound strategies., • Study Design & Protocol Development: Provide expert input on trial design, patient recruitment, and regulatory strategy to optimize study success., • Medical Oversight: Lead medical monitoring activities across assigned projects and step in as a hands-on medical monitor when needed., • Scientific Advocacy: Represent TFS at client meetings, industry conferences, and scientific events, reinforcing our reputation as a trusted CRO partner., • Medical Degree., • Board-certified in Neurology., • Deep knowledge of GCP, ICH guidelines, and regulatory requirements (FDA/EMA)., • Business acumen: Proven ability to support business development with a strategic, client-focused approach., • Exceptional communicator: Strong presentation, negotiation, and interpersonal skills for engaging stakeholders at all levels. We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients A Bit More About Us Our journey began over 25 years ago in Sweden, in the city of Lund. As a global CRO with the ultimate goal of ensuring patients’ safety and well-being, we provide biotechnology and pharmaceutical companies with tailored clinical development solutions. We currently operate in 17 countries across Europe, North America, Asia Pacific and the Middle East. Our core values of Trust, Quality, Flexibility and Passion are what make TFS Healthscience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organization. Together we make a difference. • Not Applicable, • Contract, • Health Care Provider Get notified about new Senior Medical Director jobs in Madrid, Community of Madrid, Spain . Madrid, Community of Madrid, Spain 1 month ago Madrid, Community of Madrid, Spain 1 month ago Madrid, Community of Madrid, Spain 1 month ago Madrid, Community of Madrid, Spain 1 month ago Madrid, Community of Madrid, Spain 3 weeks ago Madrid, Community of Madrid, Spain 2 weeks ago Madrid, Community of Madrid, Spain 1 week ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr

Universidad Camilo José Cela Buscamos un/a docente-investigador/a para incorporarse en nuestra institución educativa. La persona seleccionada deberá contar con un sexenio de investigación reconocido en Educación y/o Tecnología Educativa y asumirá un papel transversal en la impartición de asignaturas en diferentes titulaciones, según su perfil académico y profesional. Docencia interdisciplinar adaptada a las necesidades académicas de diversas titulaciones. • Enviar o adjuntar el reconocimiento oficial de sexenio de investigación en Educación y/o Tecnología Educativa (imprescindible)., • Experiencia en docencia universitaria y capacidad para adaptarse a diversos programas de estudios., • Incorporación a un equipo docente dinámico y comprometido con la excelencia educativa., • Oportunidad de contribuir al desarrollo académico en un entorno innovador y colaborativo. #J-18808-Ljbffr

Healthcare Recruitment Manager @ PARAGONA | Medical Recruitment Paragona has been recruiting doctors for the last 22 years. Currently, we have an offer from BELGIUM with excellent financial conditions. The salary is €24,000 per month, with the possibility to earn more. Other benefits include: • Great location (30 min from Charleroi Airport, 40 min from Brussels), • 8 weeks of holiday, • Online conference with the hospital, • Free visit to the hospital before signing the contract, • Free assistance with obtaining the license to practice, • Free assistance with finding accommodation, • Good proficiency in French, • Clear criminal record Employment type: Full-time Job function: Healthcare Provider, Hospitals and Health Care #J-18808-Ljbffr

When our values align, there's no limit to what we can achieve. Parexel is in the business of improving the world's health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values : Patients First, Quality, Respect, Empowerment & Accountability. Parexel is looking for a Medical Director with a very strong background in Ophthalmology. The role can be based remotely in select EMEA locations. The Medical Director is a medical expert with specialized therapeutic expertise and some experience across indications, clients, and drug development. They initiate and maintain medical and consultative relationships with clients, consult on early engagement and pre-award efforts, and serve as a medical monitor for contracted projects. The Medical Director may take on leadership roles by participating in initiatives, mentoring junior MDs, and / or managing a team of physicians where appropriate. Primary activities will focus on Medical Monitoring Delivery & PV Support. The medical monitor will independently deliver all medical support required for successful project delivery according to the contracted agreement with the sponsor (i.e., tasks and time per task contracted) and according to the assigned role (Global Lead Physician or Regional Lead Physician). Medical expertise and experience in Ophthalmology are essential for the medical monitor role and will be demonstrated through high-quality consultation on protocol development or drug development programs, medical review of various documents, collaboration on internal therapeutic area meetings, training module development, white papers, slide sets, publications, etc. Client relationship building & engagement, including soliciting and addressing client feedback and suggestions regarding medical study-related activities, are core skills required of the medical monitor. Business development : the medical monitor will provide medical expertise and leadership in Proposal Development Teams (PDTs) for client bid pursuit meetings. Skills • Excellent interpersonal skills, including the ability to interact well with sponsor / client counterparts, • Client-focused approach to work, • Excellent verbal and written medical communication skills, • Excellent standard of written and spoken English, • A flexible attitude with respect to work assignments and new learning, • Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail, • Experience in clinical medicine (general or specialist qualifications) with a specialty in Ophthalmology, which is expected to be kept up to date., • A background in clinical aspects of drug development, including all aspects of Medical Monitoring and study design / execution, is preferred., • Clinical practice experience, • Good knowledge of the drug development process, including drug safety, is preferred., • Experience in Pharmaceutical Medicine is preferred. J-18808-Ljbffr #J-18808-Ljbffr

Universidad Camilo José Cela Buscamos un/a docente-investigador/a para incorporarse en nuestra institución educativa. La persona seleccionada deberá contar con un sexenio de investigación reconocido en Comunicación y Nuevos Medios y asumirá un papel transversal en la impartición de asignaturas en diferentes titulaciones, según su perfil académico y profesional. Docencia interdisciplinar adaptada a las necesidades académicas de diversas titulaciones. • Enviar o adjuntar el reconocimiento oficial de sexenio de investigación en Comunicación y Nuevos Medios (imprescindible)., • Experiencia en docencia universitaria y capacidad para adaptarse a diversos programas de estudios., • Incorporación a un equipo docente dinámico y comprometido con la excelencia educativa., • Oportunidad de contribuir al desarrollo académico en un entorno innovador y colaborativo. #J-18808-Ljbffr

Importante laboratorio busca incorporar un Medical Science Liaison (MSL) en Madrid. Su objetivo principal será actuar como enlace científico entre la empresa y la comunidad médica, manteniendo relaciones con líderes de opinión y proporcionando información científica sobre los productos del laboratorio. La posición estará basada en Madrid, con desplazamientos por todo el territorio nacional. • Educación científica y médica, • Construcción de relaciones, • Soporte a ensayos clínicos, • Vigilancia científica y competitiva, • Entrenamiento interno, • Recopilación de insights médicos, • Cumplimiento regulatorio y ético, • Interesante paquete retributivo, • Acceso a plan de retribución flexible, • Incorporación a compañía líder en el sector #J-18808-Ljbffr

Universidad Camilo José Cela Buscamos un/a docente-investigador/a para incorporarse en nuestra institución educativa. La persona seleccionada deberá contar con un sexenio de investigación reconocido en Humanidades y asumirá un papel transversal en la impartición de asignaturas en diferentes titulaciones, según su perfil académico y profesional. Detalles del Puesto : • Docencia interdisciplinar adaptada a las necesidades académicas de diversas titulaciones., • Enviar o adjuntar el reconocimiento oficial de sexenio de investigación en Humanidades (imprescindible)., • Experiencia en docencia universitaria y capacidad para adaptarse a diversos programas de estudios., • Incorporación a un equipo docente dinámico y comprometido con la excelencia educativa., • Oportunidad de contribuir al desarrollo académico en un entorno innovador y colaborativo. #J-18808-Ljbffr

Social network you want to login/join with: Make a Real Impact in Infectious Diseases – Join a Leading Global Pharma as Medical Director (Iberia) Location: Madrid, Spain Travel: Up to 40% (national) Salary: Competitive + Benefits Package Start: ASAP We’re partnering with an award-winning global pharma company on the lookout for a Medical Director to lead the Iberia region and drive innovative medical strategies. This is an exciting opportunity to join a company at the forefront of Infectious Diseases. As the Medical Director for Iberia, you’ll lead the launch of a groundbreaking treatment this year, with several more innovative therapies lined up for the near future. Why This is Exciting: • Lead the Charge: Shape the medical strategy for cutting-edge treatments in Infectious Diseases., • Drive Innovation: Spearhead the launch of novel drug treatments, making a difference in patients' lives., • Build Relationships: Collaborate with leading Key External Experts (KEEs) and healthcare organizations., • MD with 7+ years of experience in Medical Affairs (preferably in Infectious/Rare Diseases)., • Strong leadership skills with proven experience managing teams and driving novel drug launches., • Fluent in Spanish and English with an understanding of the Iberian market., • Work with Global Leaders: Join a company that’s shaping the future of global healthcare., • Career Growth: Thrive in a dynamic, hybrid environment with significant personal growth opportunities. #J-18808-Ljbffr

Universidad Camilo José Cela Buscamos un/a docente-investigador/a para incorporarse en nuestra institución educativa. La persona seleccionada deberá contar con un sexenio de investigación reconocido en Sociología y asumirá un papel transversal en la impartición de asignaturas en diferentes titulaciones, según su perfil académico y profesional. Docencia interdisciplinar adaptada a las necesidades académicas de diversas titulaciones. • Enviar o adjuntar el reconocimiento oficial de sexenio de investigación en Sociología (imprescindible)., • Experiencia en docencia universitaria y capacidad para adaptarse a diversos programas de estudios., • Incorporación a un equipo docente dinámico y comprometido con la excelencia educativa., • Oportunidad de contribuir al desarrollo académico en un entorno innovador y colaborativo. #J-18808-Ljbffr

El objetivo del área de Enfermería en el Grupo Casaverde es proporcionar cuidados sanitarios necesarios a los usuarios, según las necesidades de los mismos, con el fin de mejorar o mantener la calidad de vida actual de los usuarios • Cumplir con rigurosidad los protocolos y procedimientos establecidos., • Valoración integral de los usuarios a su ingreso en el centro., • Vigilar y atender las necesidades asistenciales de los usuarios., • Programar y aplicar los cuidados de enfermería que requiera cada usuario., • Preparar y administrar los tratamientos médicos según prescripciones facultativas., • Cumplimentar las historias clínicas y registros asociados con la información relativa a los cuidados proporcionados., • Colaborar con el equipo multidisciplinar., • Garantizar el suministro de material sanitario y medicamentos en aquellos centros que no cuenten con Dirección/Coordinación de enfermería o especialista farmacéutico., • Revisión de caducidades de material sanitario y medicamentos., • Cumplimentar de manera adecuado registro de uso de medicación estupefaciente y mórficos., • Formación / Titulación minina –Grado o Diplomatura en Enfermería., • Colegiación. #J-18808-Ljbffr

Buscamos un/a docente-investigador/a para incorporarse en nuestra institución educativa. La persona seleccionada deberá contar con un sexenio de investigación reconocido en Derecho y asumirá un papel transversal en la impartición de asignaturas en diferentes titulaciones, según su perfil académico y profesional. Docencia interdisciplinar adaptada a las necesidades académicas de diversas titulaciones. • Enviar o adjuntar el reconocimiento oficial de sexenio de investigación en Derecho (imprescindible)., • Experiencia en docencia universitaria y capacidad para adaptarse a diversos programas de estudios., • Incorporación a un equipo docente dinámico y comprometido con la excelencia educativa., • Oportunidad de contribuir al desarrollo académico en un entorno innovador y colaborativo. #J-18808-Ljbffr

Buscamos un / a docente-investigador / a para incorporarseen nuestra institución educativa. La persona seleccionada deberá contar con un sexenio de investigación reconocido en Educación y / o Tecnología Educativa y asumirá un papel transversal en la impartición de asignaturas en diferentes titulaciones, según su perfil académico y profesional. Detalles del Puesto : Docencia interdisciplinar adaptada a las necesidades académicas de diversas titulaciones. • Enviar o adjuntar el reconocimiento oficial de sexenio de investigación en Educación y / o Tecnología Educativa(imprescindible)., • Experiencia en docencia universitaria y capacidad para adaptarse a diversos programas de estudios., • Incorporación a un equipo docente dinámico y comprometido con la excelencia educativa. Doctores con sexenio en Educación y/o Tecnología Educativa • Madrid, Spain #J-18808-Ljbffr

Estamos buscando formadores acreditados para impartir certificados de profesionalidad en atención sociosanitaria a personas dependientes. • Impartir contenidos teóricos y prácticos., • Dinamizar y gestionar la plataforma de formación online., • Seguir al alumnado y verificar el cumplimiento de los requisitos formativos., • Elaborar informes de seguimiento., • Acreditación oficial para impartir el certificado correspondiente., • Experiencia docente, de al menos un año., • Disponibilidad para tutorías presenciales., • Manejo fluido de plataformas de teleformación., • Competencias digitales avanzadas y dominio de herramientas informáticas., • Capacidad para elaborar material didáctico adaptado al alumnado., • Redacción de informes de seguimiento., • Responsabilidad, profesionalismo y compromiso con la calidad formativa., • Incorporarse a un equipo dinámico con impacto social real., • Modalidad mixta (teletrabajo + apoyo presencial)., • Buen ambiente y oportunidades reales de desarrollo.

We are currently seeking a highly experienced Consultant Neurologist to join a leading healthcare group in Riyadh, Saudi Arabia . This is a rare opportunity to work with a forward-thinking, multidisciplinary team dedicated to delivering world-class neurological care. In-Person Interviews – 21st May 2025 (Madrid) The hiring team will be conducting in-person interviews on 21st May 2025 in Madrid . Candidates who are able to attend in person will be given priority in the selection process. Key Responsibilities • Diagnose and manage patients with a wide range of neurological disorders., • Perform and interpret neurodiagnostic procedures including EEG, EMG, and nerve conduction studies., • Collaborate with multidisciplinary teams to deliver comprehensive, patient-focused care., • Provide leadership and mentoring to junior doctors and residents., • Participate in medical audits, research, and continuing education activities. Required : • Medical degree (MBBS or equivalent) from a recognised institution., • Board certification in Neurology (e.g., CCT (UK), American Board, Canadian Board, or equivalent)., • Minimum of 3 years' post-board certification experience in a consultant-level role., • Demonstrated expertise in managing complex neurological conditions., • Excellent communication, leadership, and patient care skills., • Subspecialty training (e.g. epilepsy, stroke, neurophysiology, MS)., • Previous experience in a tertiary hospital or internationally accredited institution., • Experience in teaching or supervision of junior medical staff., • Tax-free salary up to €300,000 PA depending on experience., • 30 days annual leave plus public holidays., • Fully furnished family accommodation., • Education allowance for up to 2 children., • Comprehensive family medical insurance (spouse and 2 children). Neurologist • Madrid, Community of Madrid, Spain #J-18808-Ljbffr

Job Title : Senior Biostatistics Expert The role of Senior Biostatistics Expert is to provide strategic statistical guidance on study design, including statistical model selection, sample size calculations, and analysis planning across clinical trials and non-interventional studies (NIS). Key responsibilities include reviewing and approving all biostatistics documentation and statistical programming outputs, overseeing project budgets and timelines, ensuring overall quality and consistency across assigned accounts. Additional duties involve contributing to talent acquisition efforts and collaborating with Quality Management to establish and maintain standard operating procedures (SOPs) and training programs. As a Senior Biostatistics Expert, you will be responsible for providing advanced statistical expertise in the planning and design of clinical trials and non-interventional studies (NIS), performing in-depth data analyses, and offering statistical guidance for study reporting. What You Will Do : • Provide strategic statistical guidance on study design, including statistical model selection, sample size calculations, and analysis planning across clinical trials and non-interventional studies (NIS)., • Lead the development and programming of statistical analyses, tables, figures, and listings (TFLs) using SAS, ensuring alignment with sponsor requirements and internal standards., • Generate and validate derived analysis datasets in compliance with CDISC ADaM standards., • Author, review, and ensure rigorous quality control (QC) of Statistical Analysis Plans (SAPs) and related statistical documentation., • Validate programming output (e.g., TFLs, datasets) generated by team members to ensure accuracy and consistency., • Provide expert statistical input to study documents, including Case Report Forms (CRFs), Data Management Plans (DMPs), and clinical protocols., • Oversee and ensure proper execution of randomization procedures., • Conduct and interpret meta-analyses using statistical results from multiple published studies, ensuring scientifically robust conclusions., • Lead the statistical review and interpretation of Clinical Study Reports (CSRs), ensuring alignment with the SAP and regulatory expectations., • Proactively prioritize and manage multiple studies and projects to meet timelines and client expectations, balancing resources and risk., • Serve as a primary statistical point of contact for internal and external stakeholders, providing clear, compliant, and insightful responses and guidance., • Ensure all statistical deliverables meet applicable regulatory standards (e.g., ICH, GCP), industry guidelines, and internal SOPs., • Foster and maintain trusted relationships with clients, leading communication on statistical matters and contributing to long-term collaboration., • Drive the continuous improvement and development of internal statistical programming practices, guidelines, and SOPs., • Mentor junior team members, contribute to training initiatives, and promote a high-performing, quality-focused team culture., • Serve as a domain expert, integrating clinical, statistical, and industry best practices to design tailored solutions for complex client needs., • Master's degree in Statistics, Biostatistics, or a related quantitative field is required with a minimum of 5-8 years of practical experience., • Minimum 5–8 years of relevant experience in biostatistics, preferably in the pharmaceutical, CRO, or life sciences sector., • Solid experience with non-interventional / observational studies and Phase 3 or Phase 4 clinical trials., • Demonstrated experience working with CDISC standards (including SDTM and ADaM)., • Good knowledge of the industrial standards (CDISC, ICH E9, GCP)., • Proficiency in SAS and R programming with a minimum of 5 years of experience with both software., • Prior experience acting as a client-facing lead statistician, including proposal support and study design., • Strong understanding of project management, including budget management, timelines, and resource allocation., • Experience mentoring or leading junior statisticians or project team members., • Excellent communication skills (written and verbal) in English., • Ability to manage multiple studies and clients simultaneously., • Strong organizational skills and attention to detail., • High level of initiative, accountability, and professionalism., • Excellent skills and knowledge of MS Office and IT., • Sound numerical reasoning., • Highly analytical with a problem-solving approach. #J-18808-Ljbffr

Requisition ID4274 -Posted -Spain -Madrid Act as a link between the Medical Affairs area and the HCP, taking a predominant scientific approach and guaranteeing that different stakeholders have access to medical and scientific information, in compliance with current and internal legislation, regulations. • Provide technical and scientific expertise (both internally and externally) under the product scope;, • Create, develop and maintain a strong, close and bi-directional scientific relationship with leading and current key opinion leaders (KOLs), opinion leaders (OL), scientific groups and other relevant external stakeholders;, • Implement and disseminate high quality medical and scientific educational programs, including acting as a speaker on scientific presentations at meetings, organized by the company or external scientific groups;, • Support the Marketing and Medical Information teams in scientific development, providing scientific training to team when necessary;, • Identify and follow-up on clinical investigation projects;, • Respond to internal and external requests/questions for medical and scientific information on marketed and / or investigational drugs;, • Collect reported adverse events and communicate them to Pharmacovigilance;, • Support the preparation of publications and reviewing of literature;, • Prepare presentations of relevant aspects of the products for medical groups;, • Contribute, upon request, in the definition of the strategic plan, as well in the promotional materials workflow approval;, • Participate in international medical affairs activities, as well as international congresses and symposia;, • Collaborate on other tasks / department activities as needed;, • Support the development and implementation of R&D activities at country level., • Master's Degree in Health Sciences, or Medical Doctor (MD);, • At least 2 year experience as MSL in Pharmaceutical industry or similar;, • Knowledge of the regulations and procedures in the Pharmaceutical Industry;, • Fluency in English (spoken and written);, • Good interpersonal skills, communication and teamwork;, • Autonomy, proactivity and good analytical skills;, • Availability to travel;, • PhD in Pharmaceutical Sciences (preferred); #J-18808-Ljbffr

• Oferta promocionada, • Oferta promocionada, • Oferta promocionada, • Oferta promocionada, • Oferta promocionada, • Oferta promocionada, • Oferta promocionada, • Oferta promocionada, • Oferta promocionada, • Oferta promocionada, • Oferta promocionada, • Oferta promocionada, • Oferta promocionada, • Oferta promocionada, • Oferta promocionada, • Oferta promocionada, • Oferta promocionada ¿Eres adaptable, compasivo y un jugador de equipo con buenas habilidades de comunicación? Contamos con muchas oportunidades para que médicos generales se unan a prácticas locales amigables y eficientes en todo el país. Estas prácticas cuentan con un excelente personal de apoyo, incluyendo enfermeros, administradores y gerentes de práctica. También están completamente informatizadas. Excelentes salarios competitivos. Contacta hoy a nuestro equipo administrativo con tu CV para conocer más sobre las oportunidades disponibles. Experiencia trabajando como médico de familia (GP) imprescindible o Especialidad en Medicina Familiar preferida. Registro en el Consejo Médico Irlandés o elegibilidad para registrarse en él. Dominio del inglés. Habilidades clave Paralegal en Propiedad Comercial, Apoyo Familiar, Ventas FMCG, Soporte Administrativo, Adobe Flash Tipo de empleo: Contrato Experiencia: años Vacantes: 1 #J-18808-Ljbffr

We drive our mobile dental practice to various care locations to treat special target groups such as the elderly, disabled, and mental health patients. Do you find fulfillment in helping people who rely on care and support on location? Are you looking for a social work environment where you, as a dentist, can make an important contribution? Then we would love to meet you! Who are we looking for? We are looking for a dentist who is seeking a new challenge with lots of freedom, responsibility, and opportunities to further develop themselves. It is possible to work full-time with us, on call, or for example, one day per week alongside your regular work. You can travel throughout the Netherlands but also work in a fixed location. Actually, everything is possible! We would like to discuss with you where your wishes and ambitions lie so that we can ensure a good fit. Working as a dentist with us means working in a professional mobile dental practice, but with vulnerable people in a constantly changing setting. At our mobile dental practice, you are responsible, along with a small and close-knit team, for the high-quality care we provide to our clients. Dental care with extras, such as special patients, emergency care, different cultures, and changing environments. Does this appeal to you? Then you are the dentist we are looking for! This is what we offer you : • A beautiful and competitive salary;, • Fulfillment; you make a big impact on the well-being of vulnerable people with the work you provide;, • Responsibility and freedom; as a dentist, you run your own mini-practice;, • Working on a self-employed basis or in employment with a fixed (hourly) rate;, • Assistance from an experienced dental assistant;, • Personal development, coaching, and support from our head office;, • You have an affinity for emergency care;, • You are available on an on-call or fixed basis;, • You have a radiation hygiene diploma 5A / M or radiation expert;, • Proactive, helpful, service- and people-oriented;, • Collegial, committed, and empathetic;, • Possess an EU / EEA Diploma in Dentistry issued by a European country or have your recognition validated for at least 3 consecutive working years in the EU country., • Demonstrate mastery of the English language at a full professional proficiency level., • Be proficient in Dutch or have the willingness to learn it through our exclusive Language Academy, with our full support. The spacious, bright vehicle is equipped with all the modern facilities that a professional dentist needs to practice their profession well. From comfortable furniture to X-ray equipment and a powerful Wi-Fi connection, there is always a fast connection possible with the location where you are working. Have we caught your attention? You can send an email to #J-18808-Ljbffr

We believe in dental care for everyone. We drive our mobile dental practice to various care locations to treat special target groups such as the elderly, disabled, and mental health patients. Do you find fulfillment in helping people who rely on care and support on location? Are you looking for a social work environment where you, as a dentist, can make an important contribution? Then we would love to meet you! Who are we looking for? We are looking for a dentist who is seeking a new challenge with lots of freedom, responsibility, and opportunities to further develop themselves. It is possible to work full-time with us, on call, or for example, one day per week alongside your regular work. You can travel throughout the Netherlands but also work in a fixed location. Actually, everything is possible! We would like to discuss with you where your wishes and ambitions lie so that we can ensure a good fit. Working as a dentist with us means working in a professional mobile dental practice, but with vulnerable people in a constantly changing setting. At mobile dental practice, you are responsible, along with a small and close-knit team, for the high-quality care we provide to our clients. Dental care with extras, such as special patients, emergency care, different cultures, and changing environments. Does this appeal to you? Then you are the dentist we are looking for! This is what we offer you: • A beautiful and competitive salary;, • Fulfillment; you make a big impact on the well-being of vulnerable people with the work you provide;, • Responsibility and freedom; as a dentist, you run your own mini-practice;, • Working on a self-employed basis or in employment with a fixed (hourly) rate;, • Assistance from an experienced dental assistant;, • Personal development, coaching, and support from our head office;, • You have an affinity for emergency care;, • You are available on an on-call or fixed basis;, • You have a radiation hygiene diploma 5A / M or radiation expert;, • Proactive, helpful, service- and people-oriented;, • Collegial, committed, and empathetic;, • Possess an EU / EEA Diploma in Dentistry issued by a European country or have your recognition validated for at least 3 consecutive working years in the EU country., • Demonstrate mastery of the English language at a full professional proficiency level., • Be proficient in Dutch or have the willingness to learn it through our exclusive Language Academy, with our full support. Have we caught your attention? You can send an email to call or send a WhatsApp at and get in touch with Eunice Lazar. She will inform you about the hiring process, and language academy and give you more details about the vacancies. #J-18808-Ljbffr

Care Force | Connecting International Medical Professionals 08 ago | Care Force | Connecting International Medical Professionals | Madrid We believe in dental care for everyone. We drive our mobile dental practice to various care locations to treat special target groups such as the elderly, disabled, and mental health patients. Do you find fulfillment in helping people who rely on care and support on location? Are you looking for a social work environment where you, as a dentist, can make an important contribution? Then we would love to meet you! We are seeking a dentist who is looking for a new challenge with lots of freedom, responsibility, and opportunities for personal development. You can work full-time, on call, or for example, one day per week alongside your regular job. You can travel throughout the Netherlands or work at a fixed location—everything is possible! We want to discuss your wishes and ambitions to ensure a good fit. Working with us means being part of a professional mobile dental practice, serving vulnerable people in a constantly changing environment. You will be responsible, along with a small, close-knit team, for providing high-quality care. Our services include emergency care, working with diverse cultures, and adapting to changing environments. If this appeals to you, you are the dentist we are looking for! • A competitive salary, • Fulfillment by making a significant impact on vulnerable people's well-being, • Responsibility and freedom to run your own mini-practice, • Work on a self-employed basis or with a fixed hourly rate, • Assistance from an experienced dental assistant, • Support from our head office, including coaching and personal development, • A versatile work environment with contacts from different cultures, • An affinity for emergency care, • Availability on an on-call or fixed basis, • A radiation hygiene diploma 5 A/M or radiation expert certification, • Proactive, helpful, service- and people-oriented attitude, • Collegial, committed, and empathetic nature, • Possession of a driver’s license and a car, • An EU/EEA Diploma in Dentistry issued by a European country or recognition validated for at least 3 years in an EU country, • Proficiency in English at a full professional level, • Willingness to learn Dutch through our exclusive Language Academy, with full support from us Contact Ana via email, phone, or WhatsApp at . She will provide details about the hiring process, language academy, and vacancies. Original ad available at: ___ #J-18808-Ljbffr

We believe in dental care for everyone. We drive our mobile dental practice to various care locations to treat special target groups such as the elderly, disabled, and mental health patients. Do you find fulfillment in helping people who rely on care and support on location? Are you looking for a social work environment where you, as a dentist, can make an important contribution? Then we would love to meet you! We are looking for a dentist seeking a new challenge with lots of freedom, responsibility, and opportunities for personal development. It is possible to work full-time, on call, or for example, one day per week alongside your regular work. You can travel throughout the Netherlands or work in a fixed location—everything is possible! We would like to discuss your wishes and ambitions to ensure a good fit. • Working in a professional mobile dental practice with vulnerable people in a constantly changing setting., • Being responsible, along with a small, close-knit team, for the high-quality care we provide., • Providing dental care with extras, such as for special patients, emergency care, and diverse cultural backgrounds., • A competitive salary;, • Fulfillment: making a significant impact on the well-being of vulnerable people;, • Responsibility and freedom: running your own mini-practice;, • Work on a self-employed basis or in employment with a fixed hourly rate;, • Assistance from an experienced dental assistant;, • Personal development, coaching, and support from our head office;, • A versatile work environment with contact with people from different cultures., • Affinity for emergency care;, • Availability on an on-call or fixed basis;, • Radiation hygiene diploma 5A / M or radiation expert;, • Proactive, helpful, service- and people-oriented;, • Collegial, committed, and empathetic;, • Possession of a driver’s license and a car., • EU / EEA Diploma in Dentistry issued by a European country or recognition validated for at least 3 years within the EU;, • Full professional proficiency in English;, • Proficiency in Dutch or willingness to learn through our Language Academy with full support; You can contact Eunice Lazar via email or WhatsApp at +40 775 235 310. She will inform you about the hiring process, language academy, and provide more details about the vacancies. #J-18808-Ljbffr

As a Medical Director you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Medical Director, Clinical Development Sciences Hematology may lead the clinical sub-team or support the clinical sub-team and the global program team to build global clinical development plans and contributes to the development of asset level and therapeutic area strategies. Responsible for overseeing the clinical development strategy development and execution for 1 program, leading the clinical subteam , contributing to the development of regulatory strategy, and representing the clinical program at regulatory meetings Responsibilities • Lead or support the clinical subteam and oversee the design and execution of multiple clinical studies or clinical programs., • Represent Clinical Development on the Global Program Team and in presentations at management and review committees., • Functionally, supervise and develop medical monitors and / or clinical development scientists, if any and as assigned by the manager., • Lead one or more clinical study teams in the preparation of clinical study related documents including protocols, charters, statistical summary reports, meeting presentations, publications, and clinical sections of regulatory documents, as assigned by manager., • Development of medical content for regulatory document, and responses (including but not limited to NDAs / BLAs, sNDAs / SBLAs, briefing packages and common technical documents), • Critically evaluate available information about diseases of interest to the therapeutic area and the competitive landscape and synthesize information succinctly to support dissemination and incorporation into clinical development programs, asset plans, and therapeutic area strategy., • Physician with MD or foreign equivalent; PhD nice to have, • 5-10 years of clinical development experience preferably within industry, • 3-5 years minimum experience as a medical monitor for clinical trials required, • Regulatory experience required, • Track record of publication in peer reviewed journals, preferably first-authored publications, • Advanced knowledge of the assigned therapy area (hematology) is desired, with the capability to interpret, discuss and represent trial or program level data., • 5+ years of industry experience in clinical development is preferred, • Experience for medical responsibilities on a cross-functional team preferred J-18808-Ljbffr #J-18808-Ljbffr

We are seeking an Allergist - Medical Director to join our dynamic team in Madrid. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. All Medical Directors have hybrid WFH flexibility. Responsibilities • Provide medical management and expertise for clinical trials;, • Contribute medical expertise to study reports, regulatory documents, and manuscripts;, • Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;, • Participate in new business development through involvement in proposal and sponsor meetings as requested;, • Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;, • Must have an M.D., specialization in Allergy and current medical licensure;, • Board certification;, • Prior clinical trial research experience preferred; Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks • Flexible work environment, • Competitive compensation and benefits package, • Competitive PTO packages, • Structured career paths with opportunities for professional growth, • Company-sponsored employee appreciation events, • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets #J-18808-Ljbffr

We are seeking an Allergist - Medical Director to join our dynamic team in Madrid. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. All Medical Directors have hybrid WFH flexibility. Responsibilities • Provide medical management and expertise for clinical trials;, • Contribute medical expertise to study reports, regulatory documents, and manuscripts;, • Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;, • Participate in new business development through involvement in proposal and sponsor meetings as requested;, • Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;, • Must have an M.D., specialization in Allergy and current medical licensure;, • Board certification;, • Prior clinical trial research experience preferred; Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? • Flexible work environment, • Competitive compensation and benefits package, • Competitive PTO packages, • Structured career paths with opportunities for professional growth, • Company-sponsored employee appreciation events, • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO / AA Employer M / F / Disability / Vets #J-18808-Ljbffr

Legit.Health deploys computer vision and artificial intelligence technology to enable lifesaving diagnosis and therapies for visible diseases. Ourgoal is to enable universal access to high-quality diagnosis and follow-up of pathologies and to offer affordable health assistance to everyone everywhere. Things you should know before following and signing up for the position : We are a startup, it is important that you are knowledgeable about how startups operate and know that at this stage there are more unknowns than certainties. There are many things to discover and define yet, so you will be part of that definition, therefore you will have many functions helping the management. At Legit.Health we have a friendly open collaborative culture and a united team vision. We love entrepreneurial / risk taking / high ambition mindsets. Our work is rewarding and we help each other win by creating a supportive and collaborative environment for one another. Take a look at our opening below and send us your application - we look forward to hearing from you! We are seeking a highly skilled and knowledgeable In-House Legal Counselor to oversee our legal department. This critical role involves managing all legal aspects of our business operations, with a particular focus on Business Law and Data Protection under GDPR. The ideal candidate will be proficient in drafting, reviewing, and negotiating contracts, and will act as our Data Protection Officer to ensure full compliance with GDPR. This position offers a unique opportunity to join a dynamic startup environment, influencing the growth and structure of our company's legal framework. What you need to achieve Contract management : Draft, review, and negotiate contracts with clients, partners, suppliers, and employees to safeguard the company’s interests. Compliance and risk management : Ensure compliance with all applicable laws and regulations, particularly in relation to business operations and data protection. Conduct risk assessments and provide proactive legal advice to mitigate potential legal issues. Data protection : Serve as the Data Protection Officer, responsible for implementing data protection strategies, managing data-related incidents, and maintaining records of processing activities in accordance with GDPR requirements. Legal advisory : Provide legal advice on a wide range of issues including intellectual property, employment law, corporate governance, and regulatory compliance. Policy development : Develop and update internal policies and procedures to reflect current laws and regulations, promoting legal and ethical integrity. Litigation management : Handle pre-litigation legal disputes and inquiries, and coordinate with external counsel as necessary to manage litigation cases. Training and development : Conduct training sessions for staff on legal compliance, particularly focusing on data protection and GDPR. Stakeholder engagement : Work closely with various departments to provide legal support and ensure compliance across all aspects of the business. Must have Juris Doctor (JD) degree or equivalent qualification in Law. Licensed to practice law in the relevant jurisdiction. Minimum of 5 years of legal experience, with a strong background in business law and data protection. Previous experience as a Data Protection Officer and thorough understanding of GDPR compliance. Experience in the technology or health sector is highly preferred. Excellent negotiation, communication, and presentation skills. Ability to handle multiple projects in a fast-paced environment. Important Able to work autonomously, with discipline and with high motivation and energy Proactive, willing to learn, have an impact and grow in the company Team player capable of adapting to changes in a fast-paced environment What do we offer ️ Full-remote position. We are a team of committed professionals, so you choose where you work from and also means that all processes need to be thought of as if we had no office and everyone is working remotely. No one will feel like an outsider, since all conversation will need to happen on slack or hangouts. Working in a fast growing Start-up environment within an international context Flexible compensation (Cobee) : daycare and restaurant Flexible vacation policy : 23 working days per year + 2 additional days granted by the company (your birthday and December 7th) + 2 days for company closure per labor agreement (December 24th and 31st) Full-time contract Starting day : as soon as possible. Competitive salary according to your experience Languages High Spanish and English proficiency (writing and speaking). Additional languages are a plus In compliance with the provisions of the data protection regulations, we inform you that the personal data you have provided with your resume will be processed in a mixed manner (automated or not) by AI Labs Group, S.L., with NIF B and address in Gran Vía, 1, BAT Tower, Bilbao (Bizkaia), 48001 (hereinafter, Legit.Health). The purpose of this data processing is the management of Legit.Health's personnel selection processes and is based on your prior consent. Your data will be kept for one year, after which we will proceed to cancel it. You are also informed that no automated decisions will be made. Your data will not be transferred to third parties. At any time you can exercise your rights of access, rectification, deletion, portability, limitation, or opposition, by writing to the email We also inform you that you can go to the Control Authority to assert your data protection rights. #J-18808-Ljbffr

We are seeking a Medical Director - Oncology/Hematology to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. **All Medical Directors have hybrid WFH flexibility. Responsibilities • Provide medical management and expertise for clinical trials;, • Contribute medical expertise to study reports, regulatory documents, and manuscripts;, • Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;, • Participate in new business development through involvement in proposal and sponsor meetings as requested;, • Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;, • Must have an M.D., specialization in Oncology/Hematology and current medical licensure;, • Board certification;, • Prior clinical trial research experience preferred; and Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks • Flexible work environment, • Competitive compensation and benefits package, • Competitive PTO packages, • Structured career paths with opportunities for professional growth, • Company-sponsored employee appreciation events, • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. • Must have an M.D., specialization in Oncology/Hematology and current medical licensure;, • Board certification;, • Prior clinical trial research experience preferred; and, • Provide medical management and expertise for clinical trials;, • Contribute medical expertise to study reports, regulatory documents, and manuscripts;, • Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;, • Participate in new business development through involvement in proposal and sponsor meetings as requested;, • Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;, • Follow specific research related protocol and lead others in strict adherence to the policies. #J-18808-Ljbffr

We are seeking a Metabolic/Endocrine - Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. **All Medical Directors have hybrid WFH flexibility. Responsibilities • Provide medical management and expertise for clinical trials;, • Contribute medical expertise to study reports, regulatory documents, and manuscripts;, • Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;, • Participate in new business development through involvement in proposal and sponsor meetings as requested;, • Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;, • Must have an M.D., specialization in Metabolic/Endocrine and current medical licensure;, • Board certification;, • Prior clinical trial research experience preferred; and Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks • Flexible work environment, • Competitive compensation and benefits package, • Competitive PTO packages, • Structured career paths with opportunities for professional growth, • Company-sponsored employee appreciation events, • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. • Must have an M.D., specialization in Metabolic/Endocrine and current medical licensure;, • Board certification;, • Prior clinical trial research experience preferred; and, • Provide medical management and expertise for clinical trials;, • Contribute medical expertise to study reports, regulatory documents, and manuscripts;, • Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;, • Participate in new business development through involvement in proposal and sponsor meetings as requested;, • Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;, • Follow specific research related protocol and lead others in strict adherence to the policies. #J-18808-Ljbffr

We are seeking a neurologist Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. **All Medical Directors have hybrid WFH flexibility. Responsibilities • Provide medical management and expertise for clinical trials;, • Contribute medical expertise to study reports, regulatory documents, and manuscripts;, • Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;, • Participate in new business development through involvement in proposal and sponsor meetings as requested;, • Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;, • Must have an M.D., specialization in neurology and current medical licensure;, • Board certification;, • Prior clinical trial research experience preferred; and Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks • Flexible work environment, • Competitive compensation and benefits package, • Competitive PTO packages, • Structured career paths with opportunities for professional growth, • Company-sponsored employee appreciation events, • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. • Must have an M.D., specialization in neurology and current medical licensure;, • Board certification;, • Prior clinical trial research experience preferred; and, • Provide medical management and expertise for clinical trials;, • Contribute medical expertise to study reports, regulatory documents, and manuscripts;, • Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;, • Participate in new business development through involvement in proposal and sponsor meetings as requested;, • Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;, • Follow specific research related protocol and lead others in strict adherence to the policies. #J-18808-Ljbffr

Join to apply for the Medical Director - Ophthalmology role at Parexel 3 days ago Be among the first 25 applicants Join to apply for the Medical Director - Ophthalmology role at Parexel Get AI-powered advice on this job and more exclusive features. Parexel is looking for a Medical Director with a very strong background in Ophthalmology. The role can be based remotely in select EMEA locations Our careers page lists all of the countries which you can see when you click to apply. The Medical Director is a medical expert with specialized therapeutic expertise and some experience across indications, clients, and drug development. They initiate and maintain medical and consultative relationships with clients, consult on early engagement and pre-award efforts, and serve as a medical monitor for contracted projects. The Medical Director may take on leadership roles by participating in initiatives, mentoring junior MDs, and / or managing a team of physicians. Primary activities will focus on Medical Monitoring Delivery & PV Support. The medical monitor will independently deliver all medical support required for successful project delivery according to the contracted agreement with the sponsor (i.E., tasks and time per task contracted) and the assigned role (Global Lead Physician or Regional Lead Physician). Medical expertise and experience in Ophthalmology are essential to the medical monitor role and will be demonstrated through high-quality consultation on protocol development, drug development programs, medical review of documents, collaboration on internal therapeutic area meetings, training module development, white papers, slide sets, publications, etc. Client Relationship Building & Engagement, including soliciting and addressing client feedback and suggestions regarding medical study-related activities, are core skills required of the medical monitor. Business Development : the medical monitor will provide medical expertise / leadership in Proposal Development Teams (PDTs) for client bid pursuit meetings. Skills Excellent interpersonal skills including the ability to interact well with sponsor / client counterparts Client-focused approach to work Excellent verbal and written medical communication skills Excellent standard of written and spoken English A flexible attitude with respect to work assignments and new learning Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail Willingness to work in a matrix environment and to value the importance of teamwork Knowledge And Experience Experience in clinical medicine (general or specialist qualifications) with a specialty in Ophthalmology, which is expected to be kept up to date. A background in clinical aspects of drug development, including all aspects of Medical Monitoring and study design / execution, preferred Clinical practice experience Good knowledge of the drug development process including drug safety, preferred Experience in Pharmaceutical Medicine, preferred Experience leading, mentoring, and managing individuals / a team, preferred Education Medically qualified in an acknowledged medical school with completion of at least a basic training in clinical medicine (residency, internship) Seniority level : Director Employment type : Full-time Job function : This job is not marked as expired. J-18808-Ljbffr #J-18808-Ljbffr

Get AI-powered advice on this job and more exclusive features. Direct message the job poster from Leadtech Group Talent Acquisition & Development Team Lead @ Leadtech Group | International Recruitment | Team Leadership At Leadtech, we've been redefining digital businesses since 2009, creating innovative online solutions that reach millions of users every month. With a diverse team of over 700 members from 23+ nationalities, we're united by a passion for creativity and collaboration. We specialize in delivering user-centric experiences across web and mobile platforms, where people can connect with our products like never before. We're proud of our global reach and committed to fostering an inclusive workplace where every individual contributes to our shared vision of bringing cutting-edge projects to life. ABOUT THE ROLE Leadtech is growing, and we're looking for a Talent Coordinator to help us streamline and enhance our hiring processes. As we expand, ensuring a smooth and efficient candidate experience is crucial to attracting top talent. We need someone organized, proactive, and passionate about supporting recruitment operations. Do you have experience coordinating hiring processes in the digital industry? If you thrive in a fast-paced environment and enjoy working closely with recruiters and hiring managers, we'd love to hear from you! YOUR MISSION As a Talent Coordinator at Leadtech, you will: • Organize and manage interview schedules for candidates, ensuring timely communication and smooth logistics between candidates and interviewers., • Keep candidates informed throughout the recruitment process, providing timely updates on next steps and interview feedback., • Maintain and update candidate information in the Applicant Tracking System (ATS), ensuring that all records are accurate and up to date., • Assist in managing internal recruitment processes by supporting the administrative management of applications and maintaining continuous communication with employees interested in the processes, helping to ensure fluidity and satisfaction., • Assist in the preparation of job offers, ensuring all relevant documents are accurate and completed in a timely manner., • Support the collection and organization of required documentation from candidates, including references, identification, and other necessary paperwork., • Coordinate with the Payroll team to ensure that new hires are properly onboarded and all payroll-related tasks are completed. We're looking for someone with a balance of hard and soft skills who can thrive in a dynamic, cross-functional environment. Here's what we'd love to see: • Previous experience in a Talent Coordinator, HR Assistant, or similar administrative role., • Strong organizational skills with the ability to manage multiple tasks and priorities., • Excellent written and verbal communication skills with attention to detail., • Familiarity with Applicant Tracking Systems (ATS) and HR software., • Ability to work collaboratively in a team-oriented environment., • Proficiency in office software (e.g., Microsoft Office, Google Suite) and other communication tools., • Strong problem-solving skills and ability to adapt in a fast-paced environment., • Experience in managing relationships with external vendors and recruitment agencies is a plus., • Strong attention to detail. Growth and career development • Benefit from a flexible schedule with flextime (7 - 9:30 a.m. start, 3:30 - 6 p.m. end) and the option of working fully remote or from our Barcelona office. Enjoy free Friday afternoons with a 7-hour workday, plus a 35-hour workweek in July and August so you can savor summer!, • Competitive salary, full-time permanent contract, and top-tier private health insurance (including dental and psychological services)., • 25 days of vacation plus your birthday off, with flexible vacation options—no blackout days!, • If you wish to come, in our office in Barcelona you'll find it complete with free coffee, fresh fruit, snacks, a game room, and a rooftop terrace with stunning Mediterranean views. Equal Employment Opportunity Employer: Leadtech is an Equal Employment Opportunity (EEO) Employer, which means we encourage applications from people with different backgrounds, interests, and personal circumstances. Our team welcomes applicants regardless of their race, gender, age, religion, nationality, sexual orientation, and/or disabilities. All we need is your high energy, skills, and willingness to be a part of a great project! Location You'll have the flexibility to choose whether you'd like to come to the office every day, from time to time, or work fully remote. We want you to find the best combination for you. If you prefer to be surrounded by amazing people, our exceptional office is in Barcelona's Blue Building, located right on the city's seafront. Besides our stunning views, you'll enjoy our office perks such as free fruit, snacks, and coffee and you'll also be able to take part in our Mario Kart and table tennis competitions. #J-18808-Ljbffr

UNIR, Universidad líder en formación online, está en continua búsqueda de personas con talento para su desarrollo en el ámbito de la docencia y la investigación. Queremos incorporar, para el próximo curso académico, profesores especializados en el ámbito de la Psicología Educativa , tanto en su rama académica como en su rama profesional. Estamos en búsqueda para el próximo Curso Académico nuevos profesores Doctores y/o Acreditados en el Área de Psicología Educativa , para impartición/corrección de clases en diferentes titulaciones como el Máster Universitario en Neuropsicología y Educación , Máster Universitario en Atención Temprana y Desarrollo Infantil , Máster Universitario en Psicopedagogía y Máster Universitario en Prevención y Mediación de conflictos en entornos educativos . • Herramientas innovadoras para el desarrollo y preparación de las clases., • Acompañamiento diario en tus funciones docentes., • Materiales y contenidos en constante actualización., • Crecimiento profesional y asesoramiento., • Unidad de Apoyo a la Acreditación para facilitar tu desarrollo académico., • Dirección y tutoría de Trabajos Fin de Máster (TFM)., • Elaboración, supervisión y corrección de exámenes y actividades evaluativas., • Impartición de clases y seguimiento académico en la titulación., • Contar con experiencia docente y/o profesional en el campo de la Docencia Superior Universitaria o áreas afines., • Dominio de metodologías activas y tecnologías emergentes aplicadas a la docencia, así como competencia digital avanzada y manejo de plataformas educativas., • Contar con Acreditación ANECA en sus diferentes niveles., • Se valorará positivamente tener concedido algún tramo de investigación evaluado positivamente por CNEAI o por alguna agencia autonómica de evaluación de la calidad (sexenio de investigación) ., • Experiencia en formación de docentes o en programas de innovación educativa. Se aceptarán candidaturas hasta el 30 de Septiembre. El Grupo EDUCATIVO está firmemente comprometido con la igualdad de oportunidades y la diversidad, logrando con ello crear un entorno libre de toda discriminación. #J-18808-Ljbffr

Do you wish to be part of an amazing, diverse team on the frontline in researching, investigating, and acting to protect the UK’s animal, plant and bee health? If so, why not join us and make a difference. As Senior Immunologist, you will plan, manage and execute research and development into the pathogenesis and immunology of veterinary viruses. The role will coordinate the immunology work and support the research strategy of the Mammalian Virology workgroup and support the disease emergency responses in the Virology Department. The Animal and Plant Health Agency (APHA) is an executive agency of the Department for Environment, Food & Rural Affairs, and works on behalf of the Scottish Government and Welsh Government. Our diverse teams of over 3,000 skilled and committed professionals come together to provide research, advice and support to UK Government for safeguarding animal, public and plant health for benefit of the environment and economy. APHA is a brilliant place to work where our people feel valued, have a voice and can be their authentic selves. We value difference and diversity, because it helps us be more innovative and make better decisions. We are dedicated to being an inclusive employer, offering equitable opportunities for all individuals. Our goal is to build a diverse workforce, and we hope to attract applications from all backgrounds and underrepresented groups. The Science Directorate (SD) delivers high quality, high impact and highly relevant multidisciplinary science. Our People are diverse, talented, engaged and inspired to deliver innovative outcomes. • Manage research projects and design approaches for scientific investigations, ensuring completion of project objectives and milestones to the customers satisfaction; delivery of science in accord with relevant Quality Assurance standard ISO9001 and within budget., • Be a member of the Workgroup’s senior scientist team, and through deputising and delegated tasks contribute to strategic planning., • Communication of science through participation in internal and external meetings, but also to ensure a high-quality programme of scientific approaches published in peer reviewed literature with high impact., • Develop and seek opportunities for the initiation of (collaborative) research proposals, both nationally and internationally specifically through accessing opportunities out with UKgov funding., • Draft applications for funding bodies and to obtain permissions for work (e.g. from Home office and HSE)., • Maintain and enhance the immunology knowledge base to support research within the workgroup and across the department., • Monitor the horizon for technological developments that may be used to develop the research programme of host-pathogen interaction in the work group., • Oversee immunology techniques across the work group. This includes training and assisting in the experimental design and execution., • Provide consultancy to stakeholders such as the Defra, but also the industry., • Supervise and provide training for members of staff, students, and visitors in the workgroup., • Ensure that self and team maintain safe operation of the laboratory, including CL3 and 4 high containment laboratories, ensuring staff are aware of and adhere to appropriate safety procedures and emphasize a culture of continuous improvement in health and safety., • Act as room officer for an immunology laboratory, implementing and maintaining good laboratory practice and standards therein., • Participate in the disease emergency response in the event of a disease outbreak and on call rota if required. #J-18808-Ljbffr

¡Estamos buscando Terapeuta Ocupacional en Madrid! Si eres Terapeuta Ocupacional , te gusta trabajar con peques y quieres formar parte de un equipo multidisciplinar referente en Atención Temprana con más de 15 años de experiencia en el sector, contáctanos. Buscamos Terapeuta Ocupacional para una jornada de 38,5 horas en nuestro centro ubicado en la zona de Madrid Río (lunes de 8:00 a 16:00, martes, miércoles y jueves de 11:45 a 20:30, y viernes de 8:00 a 14:00). La posición es para cubrir una baja de paternidad (del 26 de mayo al 31 de julio). Se ofrece la posibilidad de cubrir el horario completo o de manera parcial. Nuestros centros están en pleno crecimiento, con plazas concertadas con la CAM y plazas de carácter privado. El salario se establece según el convenio colectivo de centros y servicios de atención a las personas con discapacidad. • Intervención directa con el usuario., • Coordinación con otros profesionales. #J-18808-Ljbffr

At Genmab, we are dedicated to building extra(not)ordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees. Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so. Does this inspire you and feel like a fit? Then we would love to have you join us! The Role Our Medical Science Liaisons (MSLs) are field-based medical affairs professionals covering various countries or regions across Europe/Rest of World (EUR/RoW). The role requires scientifically trained individuals with strong clinical/scientific backgrounds and excellent communication skills. The MSL / Sr MSL will conduct dynamic medical/scientific exchange with members of the healthcare/scientific community to generate insight and foster collaborations related to both approved and investigational assets within Genmab’s Hematology and Oncology portfolio. The current role is for an MSL / Sr MSL based in Spain.National & international travel required (60% of working time). This is an exciting opportunity to be part of the passionate, high-profile, high-impact Medical Affairs (MA) team, and work in a dynamic and collaborative setting. Responsibilities Scientific Expertise: * Act as a local expert for Genmab’s areas of interest, maintaining up-to-date knowledge of our products, relevant current & evolving clinical landscapes, and the competitive environment. Medical / Scientific Exchange: * Establish and maintain enduring relationships with members of the healthcare/scientific communities who are experts in Genmab’s areas of interest. * Provide appropriate clinical and scientific information on Genmab products in a fair and balanced manner to healthcare professionals (HCPs) in response to unsolicited requests. * Gather insight on emerging data and evolving clinical practice to inform clinical development and broader strategic initiatives. * Professionally represent Genmab at selected medical/scientific conferences. * Offer local expertise to inform engagement of health technology agencies/other payers regarding the value of Genmab products. * Engage HCPs to advance advisory boards, investigator meetings, & medical education events. Clinical Trials & Research: * Collaborate with clinical development and clinical operations teams to support company-sponsored studies, including site identification, feasibility, setup, and recruitment. * Engage with investigators to advance understanding of company assets and pipeline data. * Reactively facilitate investigator-sponsored trial proposals, coordinating submission for internal review. Territory Management: * Align and execute a local territory plan in accordance with EUR/RoW & global MA objectives. * Inform local publication planning. Training & Education: * Support training of Genmab colleagues, enhancing their knowledge and understanding of clinical data and our medicines as required. Cross-Functional Collaboration: * Proactively establish effective working relationships with internal cross-functional teams (including medical, development operations, market access) and external partners. Requirements * Advanced Scientific or Medical Degree (Pharm D, PhD, MD) or relevant clinical/professional background required. * Minimum 2 years of MSL/Medical Affairs experience required, preferably in gynecologic oncology; experience of clinical trial conduct is an advantage. * Proven ability to work independently and as a team player in collaboration with numerous internal cross-functional colleagues. * Experience of product launch preferred. * Strong understanding of pharmaceutical Codes of Practice or practice and other relevant compliance regulations applicable to interactions with members of the healthcare/scientific community. * Excellent interpersonal communication and presentation skills, strong personal integrity, teamwork abilities, and patient-centric focus are essential. * Flexible, with a positive attitude, strong ability to multi-task, priorities effectively and communicate at all levels within the company. * Fluency in English required, additional European languages an advantage. * Demonstrated technical acumen including MS Office skills, ability to adopt and leverage multiple business applications. About You * You are genuinely passionate about our purpose * You bring precision and excellence to all that you do * You believe in our rooted-in-science approach to problem-solving * You are a generous collaborator who can work in teams with a broad spectrum of backgrounds * You take pride in enabling the best work of others on the team * You can grapple with the unknown and be innovative * You have experience working in a fast-growing, dynamic company (or a strong desire to) * You work hard and are not afraid to have a little fun while you do so! Locations Genmab maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you’re in one of our office spaces or working remotely, we thrive on connecting with each other to innovate. About Genmab Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab’s vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO) antibody medicines. Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com and follow us on ___ and ___. Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website ___. Please note that if you are applying for a position in the Netherlands, Genmab’s policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the contract. #J-18808-Ljbffr

At Genmab, we are dedicated to building extra(not)ordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees. Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so. Does this inspire you and feel like a fit? Then we would love to have you join us! The Role Our Medical Science Liaisons (MSLs) are field-based medical affairs professionals covering various countries or regions across Europe /Rest of World (EUR/ RoW ) . The role requires scientifically trained individuals with strong clinical /scientific backgrounds and excellent communication skills . The MSL / Sr MSL will conduct dynamic medical/scientific exchange with members of the healthcare /scientific communit y to generate insight and foster collaborations related to both approved and investigational assets within Genmab ’s Hematology and Oncology portfolio . The current role is for an MSL / Sr MSL based in Spain . National & international travel required ( 6 0 % of working time). This is an exciting opportunity to be part of the passionate, high-profile, high-impact Medical Affairs (MA) team, and work in a dynamic and collaborative setting. Responsibilities Scientific Expertise: * Act as a local expert for Genmab’s areas of interest , m aintain ing up-to-date knowledge of our products , relevant current & evolving clinical landscape s , and the competitive environment . Medical / Scientific Exchange: * Establish and maintain enduring relationships with members of the healthcare/scientific communities who are expert s in Genmab’s areas of interest. * Pr ovide appropriate clinical and scientific information on Genmab products in a fair and balanced manner to healthcare professionals (HCPs) in response to unsolicited requests . * G ather insight on emerging data and evolving clinical practice to inform clinical development and broader strategic initiatives . * Professionally represent Genmab at select ed medical / scientific conferences . * Offer local expertise to inform engagement of health technology agencies/other payers regarding the value of Genmab products . * Engage HCPs to advance advisory boards, investigator meetings, & medical education events. Clinical Trials & Research: * Collaborate with clinical development and clinical operations teams to support company-sponsored studies, including site identification, feasibility, setup, and recruitment. * Engage with investigators to advance understanding of company assets and pipeline data. * Reactively facilitate investigator-sponsored trial proposals, coordinating submission for internal review. Territory Management: * Align and execute a local territory plan in accordance with EUR/ RoW & global MA objectives . * Inform local publication planning. Training & Education: * Support training of Genmab colleagues, enhancing their knowledge and understanding of clinical data and our medicines as required . Cross-Functional Collaboration: * P roactively establish effective working relationships with internal cross-functional teams ( including medical, development operations, market access) and external partners . Requirements * Advanced Scientific or Medical Degree (Pharm D, PhD, MD) or relevant clinical /professional background required . * Minimum 2 y ear s of MSL/ Medical Affairs experience required , preferably in gynecologic o ncology ; experience of clinical trial conduct is an advantage. * Proven ability to work independently and as a team player in collaboration with numerous internal cross-functional colleagues . * Experience of product launch preferred. * Strong understanding of pharmaceutical Code s of Practice or practice and other relevant compliance regulations applicable to interactions with members of the healthcare/scientific community . * Excellent interpersonal communication and presentation skills, strong personal integrity, teamwork abilities , and patient-centric focus are essential. * Flexible, with a positive attitude, strong ability to multi - task, priorities effectively and communicate at all levels within the company . * Fluency in English required , additional European languages an advantage. * Demonstrated technical acumen including MS Office skills, ability to adopt and leverage multiple business applications . About You * You are genuinely passionate about our purpose * You bring precision and excellence to all that you do * You believe in our rooted-in-science approach to problem-solving * You are a generous collaborator who can work in teams with a broad spectrum of backgrounds * You take pride in enabling the best work of others on the team * You can grapple with the unknown and be innovative * You have experience working in a fast-growing, dynamic company (or a strong desire to) * You work hard and are not afraid to have a little fun while you do so! Locations Genmab maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you’re in one of our office spaces or working remotely, we thrive on connecting with each other to innovate. About Genmab Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab’s vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO) antibody medicines. Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com and follow us on ___ and ___. Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website ___. Please note that if you are applying for a position in the Netherlands, Genmab’s policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the contract. #J-18808-Ljbffr

Genmab Madrid, Community of Madrid, Spain Join to apply for the Senior Medical Science Liaison - Spain (EU team) role at Genmab Genmab Madrid, Community of Madrid, Spain Join to apply for the Senior Medical Science Liaison - Spain (EU team) role at Genmab At Genmab, we are dedicated to building extra(not)ordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees. Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so. Does this inspire you and feel like a fit? Then we would love to have you join us! The Role Our Medical Science Liaisons (MSLs) are field-based medical affairs professionals covering various countries or regions across Europe/Rest of World (EUR/RoW). The role requires scientifically trained individuals with strong clinical/scientific backgrounds and excellent communication skills. The MSL / Sr MSL will conduct dynamic medical/scientific exchange with members of the healthcare/scientific community to generate insight and foster collaborations related to both approved and investigational assets within Genmab’s Hematology and Oncology portfolio. The current role is for an MSL / Sr MSL based in Spain. National & international travel required (60% of working time). This is an exciting opportunity to be part of the passionate, high-profile, high-impact Medical Affairs (MA) team, and work in a dynamic and collaborative setting. Responsibilities Scientific Expertise: • Establish and maintain enduring relationships with members of the healthcare/scientific communities who are experts in Genmab’s areas of interest., • Provide appropriate clinical and scientific information on Genmab products in a fair and balanced manner to healthcare professionals (HCPs) in response to unsolicited requests., • Gather insight on emerging data and evolving clinical practice to inform clinical development and broader strategic initiatives., • Professionally represent Genmab at selected medical/scientific conferences., • Offer local expertise to inform engagement of health technology agencies/other payers regarding the value of Genmab products., • Collaborate with clinical development and clinical operations teams to support company-sponsored studies, including site identification, feasibility, setup, and recruitment., • Engage with investigators to advance understanding of company assets and pipeline data., • Align and execute a local territory plan in accordance with EUR/RoW & global MA objectives., • Advanced Scientific or Medical Degree (Pharm D, PhD, MD) or relevant clinical/professional background required., • Minimum 2 years of MSL/Medical Affairs experience required, preferably in gynecologic oncology; experience of clinical trial conduct is an advantage., • Proven ability to work independently and as a team player in collaboration with numerous internal cross-functional colleagues., • Experience of product launch preferred., • Strong understanding of pharmaceutical Codes of Practice or practice and other relevant compliance regulations applicable to interactions with members of the healthcare/scientific community., • Excellent interpersonal communication and presentation skills, strong personal integrity, teamwork abilities, and patient-centric focus are essential., • Flexible, with a positive attitude, strong ability to multi-task, priorities effectively and communicate at all levels within the company., • Fluency in English required, additional European languages an advantage., • You are genuinely passionate about our purpose, • You bring precision and excellence to all that you do, • You believe in our rooted-in-science approach to problem-solving, • You are a generous collaborator who can work in teams with a broad spectrum of backgrounds, • You take pride in enabling the best work of others on the team, • You can grapple with the unknown and be innovative, • You have experience working in a fast-growing, dynamic company (or a strong desire to), • Mid-Senior level, • Full-time Madrid, Community of Madrid, Spain 3 weeks ago Madrid, Community of Madrid, Spain 2 weeks ago Madrid, Community of Madrid, Spain 2 weeks ago Madrid, Community of Madrid, Spain 5 days ago Madrid, Community of Madrid, Spain 1 week ago Madrid, Community of Madrid, Spain 2 weeks ago Madrid, Community of Madrid, Spain 2 weeks ago Greater Madrid Metropolitan Area 21 hours ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr