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Job Title: ¿Es usted el solicitante adecuado para esta oportunidad? Descúbralo leyendo el resumen del puesto a continuación. Commercial Representative – Dentistry / Implantology Location: Spain (Madrid, Valencia, Catalonia, Andalusia, Valencian Community, Euskadi) Type of position: Independent Business Collaboration / Freelance Representative Modality: Face-to-face (clinic visits) Compensation: Commission on sales Job Description At Magdent, a dental technology company specializing in innovative solutions for implantology, we are expanding our sales network in Spain and are looking for sales representatives with experience in the dental sector. We are looking for professionals who already have their own portfolio of products or who can combine their current activity by incorporating Magdent into their regular visits to dental clinics. The objective of the position is to present and represent Magdent's product to dental clinics, implantologists and specialists, generating commercial opportunities and accompanying the process of adopting the product. Areas of interest • Madrid, • Valencian Community, • Catalonia, • Andalusia, • Euskadi, • Galicia Responsibilities • Present and represent Magdent's product at commercial visits to dental clinics., • Develop relationships with implantologists, clinic owners, and clinical teams., • Identify new business opportunities in your area., • Follow up with customers and support account growth., • Act as an ambassador for the Magdent brand in your territory. Requirements • Previous sales experience in the dental sector (implants, prosthetics, consumables, technology, etc.)., • Active client portfolio or regular access to dental clinics., • Ability to work autonomously and results-oriented., • Good communication and presentation skills., • Residence in Spain. What we offer • Flexible collaboration, ideal for representatives with their own portfolio., • Attractive compensation model, based on sales commission + commercial margin., • Innovative product, with scientific support and high clinical interest., • Commercial support, scientific material and continuous training., • Possibility of long-term growth within Magdent's commercial network. xcskxlj How to Apply If you are interested in collaborating with an innovative company and adding a differential product to your portfolio, we would love to meet you. Apply directly on LinkedIn or contact us for more information.

Nuestro cliente es una importante Multinacional del Sector Tecnológico, cuya actividad es comercialización de productos y servicios de Gestión Documental, Soluciones y Business Services enfocados a la mejora de productividad de sus clientes. Compruebe que cumple con los requisitos de habilidades para este puesto, así como con la experiencia asociada, y luego envíe su CV a continuación. Actualmente precisa la incorporación en su estructura de un/a BUSINESS DEVELOPMENT REPRESENTATIVE (BDR) para la venta de soluciones Information Management. MISIÓN: Serás responsable de identificar cuentas estratégicas, cualificar interlocutores clave y agendar reuniones de calidad para el equipo de Account Managers, contribuyendo directamente al crecimiento del pipeline comercial. Cuáles serán tus FUNCIONES: · Identificar y analizar cuentas objetivo utilizando LinkedIn Sales Navigator y Salesforce. · Ejecutar campañas de prospección mediante: email personalizado y segmentado, llamadas telefónicas, mensajes en LinkedIn,... · Cualificar cuentas y oportunidades en Salesforce, identificando interlocutores válidos para validar necesidad y potencial. · Coordinar y agendar reuniones con los Account Managers (acceso a calendarios y cierre de visitas o reuniones online). · Registrar actividad y oportunidades en CRM. · Reportar métricas de actividad, conversión y pipeline generado. QUÉ SE OFRECE: • Contrato indefinido por parte de una Multinacional líder y referente en su sector., • Interesante paquete retributivo compuesto por fijo + variable., • Beneficios: tarjeta comida, seguro vida, plataforma idiomas, jornada intensiva verano, teletrabajo 3-2,... REQUISITOS: Buscamos perfiles que aporten de 3 a 5 años de experiencia en roles de BDR, SDR o desarrollo de negocio B2B, con experiencia en venta consultiva y prospección outbound. · Valorable experiencia en sectores tecnológicos o servicios empresariales afines. · Manejo habitual de Salesforce u otro CRM · Experiencia en LinkedIn Sales Navigator · Inglés medio alto. Si te apasiona la venta consultiva en el Canal de las Grandes Cuentas, disfrutas identificando nuevos clientes y quieres crecer en un entorno multinacional dinámico y de alto impacto, nos encantará conocerte. Saleshunters es la consultora experta en Talento Comercial. Trabajamos con numerosas compañías de diversos sectores a nivel nacional. xcskxlj Nos encantaría apoyarte en tu desarrollo profesional, ofreciéndote oportunidades laborales alineadas con tu perfil. Te invitamos a registrarte en nuestra página web:

In a few words Lea atentamente toda la información sobre esta oportunidad y luego utilice el botón de solicitud de abajo para enviar su CV y su candidatura. Position: Site Engagement and Recruitment Coordinator Location: Poland Experience: Minimum of 3 years of clinical trial experience, including previous experience as a Clinical Research Coordinator, Sponsor/CRO Clinical Research Associate, Study Nurse, or Site Director. Want to know more? #Exeltis is a leader in the field of ·#Women'sHealth. It researches, innovates and creates new treatments and devices to improve the health and wellbeing of women all over the world. With a global footprint spanning more than 40 countries, Exeltis has a team of over 4,000 professionals and a global manufacturing network. Exeltis has one overarching goal: to offer women support and care throughout every single stage #OneHealth Ready to be a #Challenger? What are we looking for? A Site Engagement and Recruitment Coordinator (SERC) who uses their strong clinical trial background and awareness of site engagement and recruitment tactics to support the clinical team in effectively planning for and achieving on-time enrollment. This position achieves these goals by working with the clinical team to proactively identify opportunities and challenges related to patient recruitment and retention. Supports the Global Clinical Operations Department by engaging, developing, and maintaining relationships with clinical investigation sites and overseeing clinical trial activities to ensure quality clinical trial execution and offer innovative solutions to recruitment and operational challenges. The SERC reports to a designated Senior Clinical Project Manager. The challenge! The Site and Recruitment Coordinator’s responsibilities include, but are not limited to: • Awareness of and active participation in activities of site-related study execution of assigned studies, including feasibility, study start-up, execution, and close-out., • Early participation in and management of study planning and preparation regarding site recruitment and retention plans, enrollment projections, and anticipated barriers to achieving on-time First Patient In., • Support oversight efforts related to collaborating CRO activities, including but not limited to: o Study delivery: including but not limited to site evaluation/selection discussions, contracts/budget negotiation, regulatory/EC submissions startup, issue management, relationship management, monitoring, and site closure facilitation. o Quality oversight: Monitoring Visit Report Review; Site Visit for site quality oversight as appropriate. o Escalate performance or quality issues and support the resolution of identified issues. oFacilitate supplemental site training or other support from the Sponsor team as needed. o Support audit and inspection readiness goals for sites on assigned studies. o Assist with and follow up on-site audits, CAPA preparation, implementation, and follow-up communication. • Independently serve as a key point of contact in the country or as a global representative for one or more studies., • Drive project recruitment and retention strategy for assigned clinical trials by supporting the development of related communication to adapt, plan, and implement local study strategies for recruitment and retention., • Participation in the review and finalization of key clinical trial documents, as assigned., • Proactive and effective communication in collaboration with key internal & external stakeholders and third-party vendors. Develop partnerships (institutions and key investigator relationships) when appropriate and beneficial for the organization and/or assigned clinical trial(s)., • Lead investigational site engagement efforts: o Define and implement strategies for successfully engaging clinical sites and investigators. o Assist in identifying high-performing sites and key opinion leaders that can contribute to Exeltis forums, boards, and/or discussions. o Support sites with enrollment barriers by reinforcing protocol-specific site recruitment plans, including review and approval of advertising campaigns. o Provide operational expertise to sites through ownership/management to ensure the engagement of highly motivated clinical investigators. • Support global team by participating in or leading other tasks and projects as assigned. Attributes and Actions Related to the Role • Understanding and execution of recruitment plans, including control of digital recruitment., • Identify the top recruiters and high-quality performers using different platforms, competitive intelligence, and contacts with KOLs and institutions., • Attend TCs and MVR reviews, serve as a key point of contact with the CROs and other stakeholders, and identify recruitment issues. May lead meeting with internal and external colleagues., • Follow-up and tracking of recruitment and retention rates. Close follow-up of screening failure and dropout rates and inactive sites, followed by a proactive proposal and implementation of mitigation actions., • Periodical calls with the sites participating in clinical trials to enhance engagement and speed recruitment. Actively detect trends or issues for resolution management., • Periodical presential meetings with the leading recruiters to boost the relationship and explain the Sponsor pipeline., • Involvement in certain clinical site monitoring activities, including support in audits and RA inspections., • Work with Clinical Operations to review and approve study and site-specific recruitment materials., • Monitor weekly enrollment metrics and work alongside the clinical team to meet/exceed enrollment goals for assigned studies., • Establish and apply best practices and lessons learned across all clinical studies., • Track, analyze, and present data from central recruitment campaigns., • Attend internal and external meetings and provide updates on recruitment and site activities. Additional Contributions • Consistently meet, at minimum, other key performance indicators (KPIs), personal performance and development goals, or improvement goals defined for the role or employee., • May support clinical trials in a CRA or Sr. CRA capacity when needed, as directed, and according to the Clinical Research Associate/Senior Clinical Research Associate Job Description., • May review trip reports for CRAs or perform as Manager/Line Manager for assigned CRAs., • May be responsible for the preparation and presentation of information during Investigator Meetings or other site meetings., • Contribute to the development and maintenance of the company’s SOPs and quality control procedures., • May be requested to lead or contribute to company initiatives., • Complete other duties as assigned. What do you need? • Education: Bachelor’s degree (or international equivalent), preferably in a scientific or health-related field., • Languages: Fluent in spoken and written English. Knowledge of other languages will be an asset, particularly local languages spoken within the regions of the assigned studies. • Experience (years/area): Minimum of 3 years of clinical trial experience, including previous experience as a Clinical Research Coordinator, Sponsor/CRO Clinical Research Associate, Study Nurse, or Site Director. Prior CRA experience is essential for fulfilling flex role CRA tasks as necessary and assigned., • Specific Knowledge: Prior experience conducting clinical research, including ICH-GCP knowledge and understanding, drug/device development process, regulatory compliance, regulatory agency requirements for clinical trials in the trial regions, study start-up, or study coordination., • Travel Requirements: Required to travel approximately 40-50% of the time., • Personal Skills: Strong communication skills, ability to focus on multiple deliverables simultaneously and deliver them on time, versatility and flexibility, general management skills, strong interpersonal and people development skills, results-oriented, superior leadership skills, superb organization skills, ability to anticipate problems and solve them successfully, and team player with the ability to work productively and independently in a remote professional environment. What will the Selection process be like? Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels. Prepare well! We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test. Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process. Do you think this offer is not for you? Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting! xcskxlj #Vetpharma #InsudPharma #Challenger #Insuder #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

About Us Wall Street Oasis is the largest community focused on careers in finance, with over 1 million registered members and 20 million annual visits. The platform offers valuable resources, insights, and networking opportunities for finance professionals and aspiring candidates. Solicitar este puesto es sencillo. Desplácese hacia abajo y haga clic en "Solicitar" para ser considerado para esta posición. About the Internship Are you a student passionate about the stock market, company analysis, or investment strategies? Do you want to build skills that top employers in equity research and investment banking are looking for? Join us as an Equity Research Intern – a role designed specifically to help college students and recent graduates build real skills, produce tangible work, and prepare for high-stakes roles in the finance industry. What You’ll Do • Assist in building robust equity research reports on public companies, • Analyze financial statements and valuation metrics (P/E, EV/EBITDA, DCF, etc.), • Track company earnings, press releases, and industry trends, • Receive structured feedback to sharpen your financial analysis and modeling skills. Who Should Apply? This is ideal for: • Undergraduate students in Finance, Economics, Accounting, or related fields, • Recent graduates preparing for finance interviews, • Students seeking real experience to stand out on LinkedIn and job applications, • Curious learners who want to explore careers in equity research, investment banking, or other finance careers. xcskxlj What You’ll Gain • Real-world project experience, • Equity research report samples for your portfolio, • Weekly mentor sessions + resume/interview prep, • Remote work flexibility Additional Details • Location: Remote (Must be based in Spain), • Duration: 6–8 weeks, part-time (flexible with class schedules), • Compensation: Unpaid, but includes certificate & referral letter Ready to research like a pro? Take your first step toward Wall Street — apply now and unlock your future in finance.

Estamos contratando | Responsable de LogísticaHuelva (España) | Contrato indefinido Buscamos un/a Responsable de Logística para liderar la operativa logística end-to-end en un entorno internacional (España, Portugal y Marruecos). Tu misiónCoordinar flujos logísticos (aprovisionamiento, almacén, expediciones)Gestionar transportes nacionales e internacionalesControlar stocks, costes y proveedores logísticosResolver incidencias y garantizar el nivel de servicioSer el punto de conexión entre operaciones, ventas y dirección Perfil ideal+5 años de experiencia en logística / transporteExperiencia en entorno internacional y multi-proveedorDominio de ERP y control de costesEspañol fluido | Francés e inglés valorados Qué ofrecemosProyecto estable y estratégico28 .000 – 34.000 € brutos/añoAutonomía, impacto real y crecimiento profesionalInteresado/a? Escríbenos por LinkedIn o envía tu CV por mensaje privado.