Medical Affairs Manager

Job Title: Medical Affairs Manager

Location: Remote - Based in the Netherlands

Job Type: Full-Time Remote Consulting Business

Industry: Life Sciences

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).