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This job expired on 05/09/2026. It no longer accepts applications.
Medical Affairs Consultant – Waterloo, Belgium
Alsinova · Waterloo
Job description
About the role
Alsinova is seeking experienced Medical Affairs Consultants to support a range of client projects across the pharmaceutical and biotech sectors in Belgium. You will act as a scientific bridge between the company, healthcare professionals, and regulatory bodies, ensuring that medical information is accurate, compliant, and strategically aligned with business objectives.
Key responsibilities
- Develop and maintain deep scientific expertise across therapeutic areas relevant to client portfolios.
- Interpret and implement local pharmaceutical regulations in collaboration with Regulatory Affairs.
- Attend national and international congresses to stay current and foster scientific exchange.
- Support the creation and execution of local Medical Affairs plans and strategies.
- Provide accurate scientific information to healthcare providers and internal stakeholders.
- Identify training needs and deliver medical education to commercial and cross‑functional teams.
- Coordinate timely responses to medical information enquiries, adhering to regulatory requirements.
- Engage Key Opinion Leaders and professional societies to strengthen stakeholder relationships.
- Assist with clinical study feasibility, trial management, and disease registry initiatives.
- Oversee publication activities, ensuring compliance with SOPs and timely dissemination of data.
- Contribute to regulatory and medical affairs documentation as needed.
Required profile
- Relevant scientific degree (MD, PhD, or PharmaD) is essential.
- Minimum of 2 years experience in the biotechnology or pharmaceutical industry.
- Strong knowledge of Belgian pharmaceutical regulations.
- Proven ability to work collaboratively with cross‑functional teams.
- Excellent written and verbal communication skills.
Required skills
- Scientific expertise in therapeutic fields relevant to client projects.
- Understanding of pharmaceutical regulatory frameworks.
- Experience preparing scientific and medical information materials.
- Publication planning and execution.
- Stakeholder engagement and KOL relationship management.
- Proficiency with PowerPoint.
- Proficiency with Word.
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Alsinova
Waterloo
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