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).

Location: Veldhoven, NL

Posted Date: 6/25/2025