Director Medical Affairs
il y a 1 semaine
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 a Medical Advisor and a Medical manager, and oversee medical activities in key areas such as IBD, rheumatology, dermatology and allergy. Key Responsibilities Strategic Leadership 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. Foster a culture of scientific excellence, compliance and collaboration. 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. Supervise Investigator-Initiated Trials, Phase 4 studies and real-world evidence programs. Governance & Compliance Ensure compliance with SOPs, pharmacovigilance regulations, aRMM requirements and local legislation. Maintain oversight of medical documentation, reporting systems (e.g. Veeva) and training. Cross-functional Collaboration 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. Qualifications & Skills 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 strategic mindset and business acumen. Experience designing and overseeing clinical trials, including IITs and Phase 4 studies. Strong background in data generation and real-world evidence initiatives. Solid publication track record in peer-reviewed journals. Excellent communication and interpersonal skills. Deep understanding of compliance, PV and regulatory frameworks. 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; trilingual capability is an asset. Strong knowledge of biosimilars, immunology and therapeutic areas such as IBD, rheumatology, dermatology and oncology is a plus.
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Director of Regulatory Affairs
il y a 2 semaines
Bruxelles, Belgique CT19 Temps pleinDirector Regulatory Affairs, Europe Rare Disease Biologics EMA Filings Experience Required Remote position- time in HQ in Europe will be required for business critical requirements. ** Please note candidates must live in Belgium to be considered ** About the Company We are working with a European biotech organisation, who are developing novel therapeutics...
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(Senior) Advisor Public Affairs
il y a 3 jours
Bruxelles, Belgique Future Affairs Temps pleinSenior) Advisor Public Affairs & Strategic Communication Type: Full-time You are an experienced Public Affairs Professional eager to think big and work with high impact trailblazers from start-ups to corporates, investors and non-profits. You are an entrepreneurial mind, a self-starter and bring a creative, pragmatic growth-mindset. University-level...
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(Senior) Advisor Public Affairs
il y a 3 jours
Bruxelles, Belgique Future Affairs Temps plein(Senior) Advisor Public Affairs & Strategic Communication Location: Brussels based with travel to Rotterdam (hybrid) Type: Full-time Apply to: info(at)future-affairs.eu Start date: as soon as possible, but latest February/ March 2025 Who Are We Looking For? You are an experienced Public Affairs Professional eager to think big and work with high impact...
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Director & Chief Compliance Officer
il y a 2 semaines
Bruxelles, Belgique CT19 Temps pleinDirector Regulatory Affairs, Europe Rare Disease Biologics Remote position- time in HQ in Europe will be required for business critical requirements. ** Please note candidates must live in Belgium to be considered ** We are working with a European biotech organisation, who are developing novel therapeutics for a range of rare diseases. We are looking...
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Public Affairs Director
il y a 3 jours
Bruxelles, Belgique European Plastics Converters | EuPC Temps pleinAbout EuPC European Plastics Converters (EuPC) is the EU-level trade association representing the interests of plastics converting companies in Europe. Based in Brussels, EuPC brings together national plastics associations and European sectoral organisations, representing more than fifty thousands converting companies that supply plastic products into key...
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Specialist regulatory affairs
il y a 2 semaines
Bruxelles, Belgique Panda International Temps pleinPMCF Specialist (Medical Devices / Clinical & Regulatory Affairs) Start Date: ASAP Contract Duration: 12 months (possibility of extension) As a PMCF Specialist, you will join the Clinical and Regulatory Affairs team at a leading global healthcare company’s Medical Devices division in Diegem, Belgium. You will collaborate with cross-functional...
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Director of Planning
il y a 1 semaine
Bruxelles, Belgique Nuwhï Temps pleinAbout 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...
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Senior Director, Medical Indication Lead
il y a 7 jours
Bruxelles, Belgique CT19 Temps pleinSenior Director, Medical Indication Lead Immunology, Neurology, Rheumatology Remote role and occasional travel to HQ in Europe may be required We are working with a European biotech organisation, who are developing novel therapeutics for a range of rare diseases. This role is an exciting opportunity to join as an Indication Lead, sitting in the global...
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Executive Director
il y a 2 heures
Bruxelles, Belgique TIC Council Temps pleinImportant: Please refer to the application instructions at the end of this posting for how to apply. TIC Council is the trade association representing the Testing, Inspection and Certification sector worldwide. With offices in Brussels, Washington DC, Shanghai, New Delhi and a membership of 120 that covers more than 160 countries, the association has a truly...
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Senior Director, Medical Indication Lead
il y a 2 semaines
Bruxelles, Belgique CT19 Temps pleinSenior Director, Medical Indication Lead Immunology, Neurology, Rheumatology Remote role and occasional travel to HQ in Europe may be required Right to Work in Belgium is required About the Company We are working with a European biotech organisation, who are developing novel therapeutics for a range of rare diseases. They have achieved FDA success with a few...
