Medical Affairs Job at MSD in Europe for Medical Candidates
The medical affairs job market continues to grow as pharmaceutical companies strengthen scientific engagement and clinical strategy. An exciting opportunity is now available for a Medical Affairs Manager Cardiovascular role in Bucuresti, Romania under MSD careers. This position plays a critical role in supporting cardiovascular therapeutic strategies, engaging scientific leaders, and contributing to innovative medical jobs in Europe within the global pharmaceutical landscape.
Job Details:
- Job Title: Medical Affairs Manager Cardiovascular
- Location: Bucuresti, Romania
- Job Type: Full-time
- Job Posting End Date: 24/03/2026
About the Company:
MSD is a global healthcare leader committed to improving lives through innovative medicines, vaccines, and scientific research. Known for advancing healthcare worldwide, MSD offers exciting MSD jobs for professionals who want to contribute to meaningful medical innovation. Through strong research capabilities and global collaboration, MSD careers continue to attract talented professionals seeking impactful medical jobs in Europe and across global markets.
Job Description:
The Medical Affairs Manager – Cardiovascular is responsible for managing medical and scientific activities within the assigned therapeutic area. This medical affairs job involves developing and implementing medical strategies, collaborating with cross-functional teams, and supporting clinical and scientific initiatives related to the company’s cardiovascular portfolio.
The role also focuses on building strong relationships with scientific leaders and healthcare professionals, contributing to research initiatives, supporting medical education programs, and ensuring accurate scientific communication. As part of MSD careers, this position plays a key role in strengthening medical strategy and supporting innovation in medical jobs in Europe and global healthcare advancement.
Education & Experience:
- The position requires a Medical Degree
- Relevant prior experience in similar positions is valuable.
Skills:
- Proficient understanding of the drug development process, relevant diseases and therapies, and local medical practice.
- Demonstrate strongly ethics and integrity.
- Excellent interpersonal skills related to management of scientific leaders, interactions with KDM, representatives of local authorities.
- Collaborative problem-solving approach within the team.
- Excellent communication and presentation skills.
- Strong leadership behaviors within delivering value for customers, by understanding and meeting their needs; act with candor and courage; make rapid, disciplined decisions.
- Ability to work effectively in a matrix organization.
- Excellent understanding of company core systems, tools, and metrics.
- English on proficiency level.
Key Responsibilities:
External Interactions – Scientific and Medical
- Develop and manage a consistent and sustained dialogue with Scientific Leaders, Key decision makers, professional societies board members and other relevant for activity
- As major part of the MAM role is maintaining high level of scientific interactions and engagement with customers. Hence at least 50% of the job should be spent on customer interactions in different forms, like face-to-face meetings (whether in one-to-one engagements or during congresses, company events), e-mails, videoconferences, telephone calls.
- Plan and execute Group Input Meetings (Advisory Boards)
- Contribute to company’s sponsored meetings and CME events, including engaging Scientific Leaders as speakers, development of slide kits and giving own lecture as relevant active participation in symposia and congresses.
- Provide tailored responses to customers’ requests for Medical Information, when applicable.
Internal Interactions – Scientific and Medical/Clinical
- Provide medical and scientific training, internal medical expertise for business strategies, support/advise within the therapeutic area in cross functional teams.
- Collaborate with Market Access for access plans, reimbursement process, including input into health economics analysis/documentation.
- Provide support to pharmacovigilance (compliance with reporting requirements).
- Ensure clinical and scientific accuracy of medical materials through effective execution of the worldwide review process, as applicable.
