
10,000+ employees
Founded 1972
💊 Pharmaceuticals
⚕️ Healthcare Insurance
🧬 Biotechnology
💰 Debt Financing on 2023-05
Pharmaceuticals • Healthcare Insurance • Biotechnology
Eurofarma is a pharmaceutical company that has been caring for health for over 50 years, focusing on a wide range of medical products, including prescription drugs, generics, and oncological medicines. They emphasize innovation through biotechnology and clinical research, and they maintain a commitment to sustainability and corporate responsibility. Eurofarma operates in multiple countries and supports healthcare professionals and consumers through comprehensive educational initiatives and accessible products.
🕒 June 1
🗣️🇧🇷🇵🇹 Portuguese Required
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10,000+ employees
Founded 1972
💊 Pharmaceuticals
⚕️ Healthcare Insurance
🧬 Biotechnology
💰 Debt Financing on 2023-05
Pharmaceuticals • Healthcare Insurance • Biotechnology
Eurofarma is a pharmaceutical company that has been caring for health for over 50 years, focusing on a wide range of medical products, including prescription drugs, generics, and oncological medicines. They emphasize innovation through biotechnology and clinical research, and they maintain a commitment to sustainability and corporate responsibility. Eurofarma operates in multiple countries and supports healthcare professionals and consumers through comprehensive educational initiatives and accessible products.
• Critical analysis of the medical literature. • Provide and make available medical-scientific expertise to support the company’s strategic decision-making. • Identify unmet needs and propose product improvements and lifecycle strategies. • Prepare and/or review medical rationale documents related to Eurofarma products. • Plan and implement medical-scientific activities for the therapeutic areas under your management. • Review and adapt, as required by local regulations, technical-scientific documents and materials, including the clinical portion of dossiers for product registration (and renewal). • Prepare the technical-scientific content of local product package inserts and review and approve the final document. • Identify and develop relationships with local, national, regional and international key opinion leaders (KOLs), medical societies and relevant patient associations. • Participate in national and international scientific events to update and disseminate clinical knowledge and to strengthen relationships with specialists. • Coordinate scientific committees. • Work with access teams, providing scientific support, connecting relevant stakeholders (KOLs, managers and providers), presenting clinical data and supporting continuing medical education initiatives. • Participate in planning and executing speaker training, including development of scientific materials, selection and engagement of speakers in collaboration with medical leadership, structuring training sessions and pre-sharing scientific content. • Train internal and external audiences on diseases and treatments, including structured support for sales force training through content development and lectures. • Plan and implement medical-clinical trainings, including support for CAE and INFOMED. • Develop and provide scripts addressing the main product objections for which you are responsible. • Support activities related to product launches, including technical-scientific support, participation in strategic planning, structuring launch events, suggesting and inviting KOLs and speakers, and potentially delivering lectures. • Plan and participate in scientific events (lectures, symposia, congresses and meetings), including selection and nomination of KOLs, suggesting speakers and scientific topics, as well as delivering lectures and moderating discussions. • Maintain direct interface with prescribers, responding to medical-scientific questions related to products. • Review investigator-initiated study requests and Phase IV study requests, follow progress and publish local clinical studies. • Clinically assess adverse events, providing technical-scientific rationale and monitoring risk/benefit. • Participate in and support pharmacovigilance activities. • Participate in internal and external safety committees. • Review and approve promotional materials, ensuring regulatory and scientific compliance.
• Degree in Medicine with medical residency and/or specialization in clinical specialties. • Active CRM (Brazilian medical license). • Proficient with Microsoft Office; experience with scientific databases. • Availability for primarily domestic travel and/or international travel (up to 60% of the time). • Broad technical-scientific knowledge, including scientific methodology, clinical research and evidence-based medicine. • Advanced English. • Basic Spanish. • Prior experience in Medical Affairs within the pharmaceutical industry is desirable, with autonomy to lead multidisciplinary projects; experience in review/approval of promotional material and relationship building with KOLs.
• Health insurance. • Dental insurance. • Meal allowance. • On-site cafeteria. • Commuting allowance / company shuttle / parking – depending on work location. • On-site pharmacy/dispensary with free medications for you, parents, spouse and children. • Life insurance. • Private pension plan to help you plan your future. • Childcare benefit (depending on work location). • On-site salon for personal care. • On-site gym to support your health. • Short Friday to enjoy the day as you wish (6-hour workday for employees not on shift schedules). • Development programs, including partnerships with educational institutions offering discounts. • Extended maternity leave. • Extended paternity leave.
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