Monitor hinchables - ferias-mercados

The Vendor Manager (VM) is responsible for establishing and managing project supplier and vendor scope, timelines, and costs for awarded opportunities throughout the project life cycle, including the execution of work orders and change orders. Additionally, the VM will ensure ongoing operational and financial oversight, and risk and issue management of vendors. The Vendor Manager acts as the project main point of contact vendors and is a client-facing member of the team who works in close collaboration with the global project team to ensure the quality delivery of vendor services. This role is perfect for you if you: • Have at least 3 years of experience in clinical research and in the biotechnology, pharmaceutical, and/or CRO industry., • Are a nimble learner, agile and creative team member, • Are a good communicator and fair conflict manager More specifically, the Vendor Manager will: • Oversee and manage study specific vendors throughout the project life cycle (i.e., start-up, conduct, and closeout)., • Review vendor contracts and ensure study requirements are captured and represented in the vendor contractual documentation. Manage and monitor vendor contract compliance; prepare change order for out-of-scope services (renewal, prolongation of agreement, new services) for ongoing studies., • Manage and control vendor project budget, scope, and timelines in partnership with the PM., • Collaborate with Indero SMEs to ensure clarity of specifications for vendors., • Develop and maintain the project Vendor Management Plan, in collaboration with relevant stakeholders., • Analyze discrepancies between planned and actual results and participate in the development of corrective actions to be taken as needed., • Lead project-specific vendor meetings, attend, and participate in internal and client facing project meetings., • Manage the quality of work done by vendors, and support vendor performance assessments., • Perform ongoing risk management activities, work with relevant business units to facilitate issue resolution with vendors., • Oversee and manage vendor project specific non-conformance and CAPAs, consult with Quality Assurance as needed., • Resolve vendor, project team, and sponsor complaints and escalations., • Maintain service controls by applying lessons learned and vendor performance assessments to ensure vendors meet the Project standards., • Review, manage and verify vendor invoices to ensure billing is appropriate based on the terms of the WO/CO of each project., • Manage vendor technological systems that track the shipment, inventory, and supply of project materials and/or data., • Collect, review and analyze project specific KPIs as applicable., • Ensure appropriateness and timeliness of filing of applicable vendor-related documents in study eTMF. Other VMO Responsibilities: • Participates in functional and/or corporate initiatives and special projects, as assigned., • May participate in business development opportunities (e.g. strategy meetings, bid defense meetings)., • May participate in identification and assessment of new vendors for qualification., • VMO team member back-up for planned and unplanned absences, as assigned. IDEAL PROFILE Education • Bachelor degree in science or relevant field of study Experience • At least 3 years of Experience in clinical research and in the biotechnology, pharmaceutical, and/or CRO industry., • Project management experience. PMP Certification is an asset., • Good knowledge of good clinical practices, and applicable Health Canada, Food and Drug Administration (FDA) regulations/guidelines as well as European Union (EU) pharmaceutical legislation for the Clinical Trials Regulation (CTR)., • Dermatology, aesthetics, and/or rheumatology experience is an asset. Skills and knowledge • Communication: Excellent verbal and written communication skills. Must be able to communicate effectively and understand stakeholder motivations and emotions. Service focus to Sponsor, Sites and Patients stakeholders., • Management: Highly organized and detail-oriented with effective project planning and time management skills. Quick learner, good adaptability and versatile. Proven competency in fast-paced and matrix environment., • Networking: Demonstrates an aptitude for connecting with others and building relationships with team members and stakeholders., • Negotiation: Negotiation and conflict management skills, appropriately assertive to advocate fairly for Indero and Client best interests., • Risk Management: Ability to identify, mitigate or control threats to the project., • Technical and digital aptitude: Use of business platforms to capture business intelligence., • Data management & analytics: Problem solver with a strong analytical mindset. Ability to gather, clean and interpret data, including KPIs.

¿Eres titulado/a superior en PRL?¿Te apasiona la docencia? Desde la Universidad Europea de Madrid estamos seleccionando profesores/as para tutorizar TFMs en nuestro máster en PRL. ¿Qué buscamos? Titulados/as superiores en PRL, en sus tres especialidades con experiencia profesional y docente contrastada. Requisitos: • Muy deseable Doctores/as o Doctorandos/as, • Muy valorable Acreditación por la ANECA, • Muy valorable tener acreditado un Sexenio de investigación, • Experiencia profesional y docente contrastada, • Docencia online, • Disponibilidad inmediata ¿Qué ofrecemos? • Formar parte de una empresa líder en su sector y en constante crecimiento., • Gran ambiente laboral, • Contrato a tiempo parcial No esperes más ¡Estamos deseando conocerte!

El Departamento de Economía de la Universidad Antonio de Nebrija, precisa incorporar un Investigador/a altamente cualificado para unirse a su equipo. El candidato/a deberá contar con un doctorado en Economía o una disciplina afín. Se valorará especialmente un sólido historial de publicaciones en revistas JCR y la capacidad de contribuir al desarrollo académico y estratégico del departamento. Responsabilidades Principales • Realizar investigaciones de alto impacto en el ámbito de la microeconometría aplicada y/o métodos cuantitativos basados en Inteligencia Artificial, con un enfoque en áreas como: bienestar individual, pobreza energética, privación material o salud., • Impartir y desarrollar asignaturas en programas de grado y posgrado, en español e inglés., • Integrarse plenamente en las actividades del Grupo de Investigación Nebrija en Economía, Bienestar, Empresa e Internacionalización (ECEMIN) colaborando activamente en sus proyectos y líneas de trabajo prioritarias., • Supervisar a doctorandos y fomentar un entorno académico centrado en la investigación., • Obtener financiación competitiva a nivel nacional e internacional. Requisitos • Doctorado en Economía, Ingeniería, Matemática o disciplinas relacionadas., • Historial probado de publicaciones en revistas científicas de alto impacto (JCR)., • Capacidad demostrada para impartir docencia de calidad en español e inglés., • Experiencia en desarrollar investigación rigurosa y relevante para la formulación de políticas.

Hartmann Young is retained with a private equity-backed, European mid-sized CRO to appoint a Chief Commercial Officer. This is a strategic role, leading a high-performing commercial team across Europe, working closely with senior leadership to define commercial strategy, drive revenue growth, and elevate client engagement across clinical services. We are looking for: • 15 years’ CRO experience (Phase I-III focus), • Experience working closely with C-level executives and PE stakeholders, • Strong commercial and strategic skill set, • Proven leadership of high performing teams, • Define & implement Sales & Marketing strategy If this position is of interest to you, please apply via the link or reach out to me for a confidential discussion

Think Ahead Education is a group in the international education sector with three education branches: Virtus, the most personalised British Sixth Form College in the Spanish market; Think Ahead Academy, a top academic support centre in Madrid; and IB Wave, our online tutoring platform that connects IB students with the best tutors. We’re on the loom out for vibrant Subject Specialists to join our dynamic team and revolutionise education with us. We’re not just teaching; we’re inspiring, challenging, and empowering the next generation. Key Responsibilities: • Weekly face-to-face lessons (max. 5 students per group)., • Full commitment toward our methodology and active participation in developing and rolling out innovative educational actions., • Plan, evaluate, and revise curriculum, course content, materials, and instruction methods., • Prepare course materials such as syllabi, homework assignments, and handouts., • Evaluating student performance and continuous feedback with the Coordinators and Head Centre., • Maintain student attendance records, grades, and other required records. Requirements: • Bachelor’s degree or equivalent in English Language., • 1 year + of teaching experience., • Native English speaking and writing., • Excellent creative, communication, and presentation skills., • Engaging personality and teaching style. What do we offer? Salary: The fee varies from 20 euros/hour to 50 euros/hour depending on the number of students. Schedule: • Afternoons from 5:15 pm to 9:15 pm. Locations: Alcobendas/Madrid/Pozuelo/Online. All our team members are trained and guided through the teaching process and supported with a great variety of educational resources. We also believe in diversity when it comes to teaching and understand that every teacher must apply our method in the way that suits him/her best. Ready to revolutionise education? We want to hear from you!

A MagmaCultura estem compromesos amb la cultura. Som un referent en el desenvolupament i gestió de projectes culturals, educatius i turístics. La nostra passió és promoure el valor de la cultura i fer-la accessible a les persones. El nostre motor principal és la professionalitat, el talent i el compromís del nostre equip expert en gestió cultural. Un dels principals valors de MagmaCultura consisteix en la creació d'un lloc de treball en el qual totes les persones se sentin respectades, representades i incloses en un entorn segur en el qual puguin desenvolupar i impulsar la seva carrera professional amb èxit. Per això mateix, com a institució compromesa amb la cultura i la diversitat, vetllem per la promoció d'un ambient de treball en el qual destaqui la igualtat de gènere i el respecte per motius de raça, ètnia, sexe, orientació sexual o diversitat funcional. T'apassiona la ciència, l'art i la cultura? Tens ganes de formar part d'un projecte innovador i dinamitzar l'experiència del públic? T'estem buscant, envia'ns la teva candidatura! Volem incorporar un/a Educador/ora - Divulgador/ora científic/a per un prestigiós equipament cultural de Lleida, amb la missió de fer visites guiades i tallers educatius, adaptant els continguts a diferents públics i fomentant l'aprenentatge interactiu en un entorn inspirador. Imagina't com serà el teu dia a dia: -Dissenyar i dur a terme tallers i activitats educatives de divulgació científica per a diversos públics, especialment per a grups escolars i familiars (visites guiades, tallers i altres activitats educatives en l’àmbit de la ciència i la tecnologia). -Adaptar i transformar els continguts perquè cada públic visqui una experiència educativa única i enriquidora, fomentant la curiositat i el pensament crític. -Preparar l'espai i el material necessaris per a la realització dels diferents tallers i activitats. -Resoldre dubtes i apropar el coneixement científic a tots els públics amb entusiasme i dinamisme. Requisits: • Ser una persona amb destacades habilitats comunicatives, orientada al servei, amb capacitat de resolució d'incidències, treball en equip i apassionada per la cultura., • Formació en Ciències: Geologia, Biologia, Ciències Ambientals, Física i/o equivalents., • Idiomes: català i castellà nadiu/bilingüe, anglès avançat per a fer visites i adaptar el guió a aquesta llengua., • Experiència prèvia en realització de visites, tallers i/o docència. Valorable posseir experiència en educació en museus i/o centres culturals., • El més important: ser una persona amb entusiasme i amb capacitat de fer viure experiències úniques a través de la ciència, l'art i la cultura. Què t'oferim: • Oportunitat d'incorporar-te a un equip líder en la gestió cultural, compromès amb la promoció del valor del patrimoni cultural i fer-lo accessible per a les persones., • Formació i aprenentatge continuat: creixeràs en un entorn que et convidarà a prendre petites decisions diàriament i on equivocar-se també forma part del procés., • Contracte: fixe discontinu., • Jornada i horari laboral: mínim 3 h/setmanals: Tenir disponibilitat per a treballar dissabtes, diumenges i festius, dins de la següent franja horària d'11:00 h a 14:00 h i 17:00 h a 20:00 h., • Incorporació: setembre 2025., • Lloc del centre de treball: Lleida.

Precision for Medicine is growing! We are hiring Manager, Clinical Monitoring to join our European team. The position could be covered fully remotely from the UK or Spain. Position Summary • The Manager Clinical Monitoring (GCM) offers an additional development path for clinical research professionals. Responsibilities are focused on the management and career development of the organization’s Clinical Research Associate (CRA) workforce as well as supporting the development of departmental initiatives to strengthen the quality and productivity of GCM operations., • This position requires the ability to independently lead, manage, and motivate a team of CRAs (employee and/or consultant) to a standard consistent with Precision for Medicine’s values and overall focus on quality. Specific focus will be to ensure the right resources are assigned to projects and that those resources have the tools necessary to be successful. In addition, this position will provide the CRAs with career development and support, to minimize turnover and maintain high levels of employee satisfaction Essential functions of the job include but are not limited to: • Generate action plans and provide developmental/strategic oversight to optimize CRA services, with a focus on high quality delivery of individual/team/departmental goals., • Assist with and contribute to project resourcing to ensure proper level and allocation resource is assigned for each project within their hierarchy (with respect to project phase). Update tracking systems and interface with project teams., • Collaborate with the Clinical Team Leads/Clinical Trial Managers and Clinical Operations Management Team to ensure that resource needs and site requirements are met appropriately., • Develop, mentor, manage and coach CRA staff to progress their skills so that Precision for Medicine quality standards are maintained. Advocate individual career development, and individual responsibility/accountability., • Perform accompanied site visits to assess CRA skills and developmental needs, as well as assist CRAs with project specific issues., • Identify quality risks and issues and recommend corrective action plans as needed to leadership team to address deficiencies in performance of employees., • Ensure that all staff have the proper resources, training, materials, and access to systems to deliver on the expectations of their position., • Ensure CRAs provide timely and accurate updates of all required administrative material (SOPs, T&E, etc.) on company systems., • Work with the Clinical Operations Management Team to continually improve and enhance CRA expectations and procedures to promote quality, consistency and efficiency in execution., • Develop and maintain metrics pertinent to CRA resource oversight, and work with Clinical Operations Management Team on the evaluation of these metrics., • Participate in the interview process for new CRAs by conducting CV review and participating in the interviewing process., • Conduct on-boarding training for new CRA staff in conjunction with Human Resources, Clinical Training and other functional areas., • Represent Precision for Medicine in a professional manner, • Manage CRA staff in accordance with Precision for Medicine’s values and policies., • Secondary responsibilities include assisting with the planning, assigning, and directing of work as well as gathering performance feedback to contribute to appropriate action plans., • Perform other duties as assigned by Leadership Qualifications • Graduate, postgraduate, 4-year college degree, or equivalent experience ideally in a scientific or healthcare discipline., • Fluent in English and French, • At least 7 years or more in clinical operations, data management or related discipline either in CRO or Pharmaceutical industry with a minimum of 5 years onsite monitoring experience. Monitoring experience includes use of electronic data capture systems as well as paper and electronic medical records., • Strong monitoring experience in oncological clinical trials., • 3-5 years of direct supervisory experience managing CRAs is expected in candidates for this position including:, • Experience creating effective development programs for clinical staff., • Experience developing evaluation processes, performing gap analysis, and ensuring all clinical staff are properly trained to perform their duties consistent with Precision for Medicine quality standards, • Ability to drive and availability for domestic and international travel including overnight stays, with an expectation of travel approximately 25%. Skills And Competencies • Demonstrates mastery knowledge of ICH-GCP, applicable local regulatory requirements, relevant Precision for Medicine SOPs, technical CRA knowledge of all phases of study (including remote monitoring and clinical data review) as well as regulatory guidance., • High capacity for Emotional Intelligence and a passion for people management and development., • As part of overall line management responsibilities, ability to develop training plans and hold personnel accountable to achieving training goals or addressing training needs, • Deep knowledge of how clinical research centers operate along with the ability to teach CRAs to solve site and execution related problems at the site level., • Demonstrates understanding and ability to work with EMRs and EDCs, • Exhibits high self-motivation and is able to work and plan independently as well as in a team environment., • Motivates other members of the project team to meet timelines and project goals., • Highly organized, ability to set priorities and possesses excellent problem-solving skills., • Focuses on continuous improvement, including the ability to make proactive assessments on how to make processes more efficient and people more effective., • Demonstrates a high degree of professionalism, as evidenced by punctuality, ability to deliver on commitments, an understanding of the service culture and positive interactions with customers and teammates, including good interpersonal skills., • Conducts formal presentations to a wide variety of audiences including colleagues, investigative staff, and clients with a high level of proficiency. Any data provided as a part of this application will be stored in accordance with our ___ For CA applicants, please also refer to our ___. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at . It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.