Medical Manager – Mid-level

Eurofarma

Médico(a) Gerente com foco em acesso à saúde na Eurofarma. Responsável por garantir a conformidade científica e o suporte médico na indústria farmacêutica.

Posted 6/1/2026full-timeSão Paulo • 🇧🇷 BrazilMid-LevelSeniorWebsite

About the role

Key responsibilities & impact

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.

Requirements

What you’ll need

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.

Benefits

Comp & perks

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.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

critical analysismedical-scientific expertiseproduct improvementsclinical researchevidence-based medicinemedical rationale documentstechnical-scientific contentadverse events assessmentpharmacovigilancepromotional material review

Soft Skills

relationship buildingcommunicationtrainingcoordinationstrategic planningleadershippresentationcollaborationautonomyproblem-solving

Certifications

Degree in Medicinemedical residencyspecialization in clinical specialtiesactive CRM (Brazilian medical license)