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Director of planning - remote

Bruxelles
Nuwhï
Publiée le Publiée il y a 5 h
Description de l'offre

About the role A fast-growing biopharmaceutical organization is expanding its Medical Affairs team and is looking for a Medical Lead for Belgium and Luxembourg. The company is known for its strong focus on biosimilars, biologics and innovative therapies, bringing high-quality and affordable treatments to patients across multiple therapeutic areas.
In this role, you will lead the Medical Affairs function, provide strategic direction and ensure scientific and regulatory excellence. You will manage a team of Medical Advisors and MSLs, and oversee medical activities in key areas such as IBD, rheumatology, dermatology and allergy.

Define and execute the local medical strategy in alignment with global and regional objectives.
Lead medical launch planning and lifecycle management activities.
Represent Medical Affairs in cross-functional leadership teams and build trusted relationships with hospital pharmacists and buying groups.

Team Management
Lead, mentor and develop a high-performing team of Medical Advisors and MSLs.
Provide oversight on supply chain planning from a medical perspective.

Scientific & Medical Oversight
Ensure high-quality scientific exchange with external stakeholders.
Oversee the medical review and approval of both promotional and non-promotional materials.
Maintain oversight of medical documentation, reporting systems (e.g. Veeva) and training.

Partner closely with Market Access, Regulatory, Commercial and Pharmacovigilance teams.
Contribute to brand planning, advisory boards and KOL engagement strategies.

Budget & Resource Management
Manage the medical budget, including grants, consultancy fees and training.
Allocate resources effectively and support strategic roadmap planning.

Advanced degree in Life Sciences (MD, PharmD or PhD preferred).
Minimum 5–7 years of experience in Medical Affairs within pharma or biotech.
Proven leadership experience and ability to manage cross-functional projects.
Strong background in data generation and real-world evidence initiatives.
Solid publication track record in peer-reviewed journals.
Ability to manage multiple priorities in a fast-paced environment.
Proficiency with medical and CRM tools (e.g. Veeva, Salesforce).
Fluency in English and either Dutch or French;

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