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Safety Evidence Medical Lead
Partnering with one of Europe’s leading immunology companies, we are looking for a physician to define how its therapies stand out on safety. As the label expands and the market crowds, the question becomes: how does the safety profile compare with current and emerging therapies, and what evidence will prove it? This role answers it. You’ll be hands-on and strategic in an evolving function, turning safety data into evidence that shapes how products are positioned for patients and prescribers.
Biotechnical
Clinical Research
Zwijnaarde - Belgium
40 hours per week
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Your consultant
About your role
This is how you will make the difference
- Identifying evidence gaps and building the safety differentiation elements of integrated evidence generation plans, with RWE/HEOR, Global Patient Safety and cross-functional partners
- Assessing the company’s products against current and emerging therapies to pinpoint differentiating attributes and evidence needs
- Designing real-world safety studies with pharmacoepidemiologists, and judging whether data sources are truly fit for purpose
- Interpreting safety evidence from multiple sources, including AI-supported outputs, with the medical judgment to know where those outputs fall short
- Turning findings into clear scientific narratives for decision-makers and publications
- Acting as the trusted safety evidence advisor to non-safety functions on study design, endpoints and interpretation
- Representing the company with key opinion leaders, treating physicians, regulators and external partners
- Testing and applying new digital and AI-enabled approaches to safety insight generation
what's needed
What you bring
- Hold a medical degree and have 10+ years in pharma or biotech, including strategic leadership in clinical development, Medical Affairs, pharmacoepidemiology or patient safety
- Have designed, interpreted or applied evidence from post-authorisation, observational or real-world studies; direct safety evidence experience is a strong plus
- Bring a scientific track record, such as peer-reviewed publications or conference presentations
- Know immunology; immunoglobulin experience is a real advantage
- Are comfortable with ambiguity: you handle unfamiliar problems, combine approaches creatively and work with limited supervision
- Use generative AI and digital tools in your work, and understand their governance and limitations
- Have working knowledge of GCP and GVP
- Located in Switzerland, Belgium, or East Coast U.S.
What we offer
What's in it for you
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