jobid=A.0.0503
Medical Affairs Manager, ‘s-hertogenbosch
Client:
Discover International
Location:
‘s-hertogenbosch, Netherlands
Job Category:
Other
–
EU work permit required:
Yes
Job Views:
2
Posted:
02.06.2025
Expiry Date:
17.07.2025
Job Description:
Job Title: Medical Affairs Manager
Location: Remote – Based in the Netherlands
Job Type: Full-Time | Remote | Consulting Business
About the Role
We are seeking a highly motivated and experienced Medical Affairs Manager to join our dynamic consulting team. Operating remotely within the Netherlands, you will play a pivotal role in supporting medical strategy and execution across multiple client projects within the pharmaceutical, biotechnology, and healthcare sectors. This position offers the opportunity to work in a fast-paced, project-based environment with cross-functional teams and international clients.
Key Responsibilities
- Develop and implement medical affairs strategies aligned with client goals and therapeutic area objectives.
- Provide scientific and medical expertise across therapeutic areas to internal stakeholders and clients.
- Support clinical development, medical information, and regulatory activities as required.
- Coordinate and lead scientific communications, including medical writing, publication planning, and review of promotional and non-promotional materials for compliance.
- Engage with key opinion leaders (KOLs), healthcare professionals (HCPs), and advisory boards to gather insights and support client needs.
- Deliver medical training and scientific support to commercial teams.
- Ensure compliance with local and international regulatory guidelines, industry codes, and internal policies.
- Stay up-to-date with scientific literature and competitive landscape relevant to client projects.
Qualifications
- Advanced degree in life sciences (MD, PharmD, PhD, or equivalent).
- Minimum of 3–5 years of experience in Medical Affairs or a similar role within the pharmaceutical, biotech, or healthcare consultancy sector.
- Strong understanding of medical affairs functions including clinical development, regulatory frameworks, and medical communications.
- Experience in cross-functional collaboration and managing external stakeholders.
- Ability to work independently in a remote environment while managing multiple projects and deadlines.
- Familiarity with EU regulatory and compliance standards (e.g., EFPIA, GDPR, local Dutch regulations).
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