Medical Affairs Manager UK & BeNeLux

J283067_1714032748 Belgium €100K / Year

Join our client's dynamic team in Brussels, a leading player in the medical industry, committed to innovation and patient safety.

We are currently seeking a motivated and experienced Medical Affairs Manager to oversee operations in the UK and BeNeLux regions. If you are passionate about pharmaceutical regulations, safety, and compliance, this could be the opportunity for you!

Territory Details

• United Kingdom & BeNeLux

Key Duties

Responsibilities:

• Implement Pharmacovigilance (PV) policies in alignment with corporate strategy, ensuring local compliance with regulations and quality standards.
• Manage local scientific and regulatory intelligence in PV, evaluating and mitigating risks associated with clinical product use.
• Serve as the primary contact for regulatory affairs (RA), overseeing submissions, variations, and renewals for marketing authorizations.
• Manage product quality complaints and ensure compliance with good practices (GMP, GDP, GCP).
• Review and approve promotional materials, provide scientific support to sales and marketing teams, and deliver product-related scientific training.
• Provide medical information to customers, participate in medical information networks, and engage with key opinion leaders.
• Oversee clinical studies, liaising with authorities and ethical committees, and managing investigator-initiated studies.
• Fulfill specific responsibilities for the BeNeLux region, including serving as the local Qualified Person in Pharmacovigilance (QPPV) and Responsible for Information and Publicity (RIP) in Belgium.

Package and Benefits

• annual base salary up to €100,000.- DOE
• 10% bonus
• company car
• benefits

Key Skills, Qualifications and Client Requirements

• Pharmacist or medical doctor with extensive experience and qualifications to oversee PV and RA activities, along with proficiency in administrative tasks related to clinical studies.
• Strong knowledge in contrast media and medical devices is advantageous.
• Essential to hold a relevant scientific degree (MD, PhD, or PharmaD).
• Minimum of 5 years of experience in the biotechnology/pharmaceutical field.
• Proficient in English, Dutch, and French, both spoken and written.
• Prior experience as a medical affairs manager is essential.
• Demonstrated success in building relationships within the industry.
• Ability to effectively present complex scientific data.
• Previous exposure to complex matrix organizations or virtual team environments is beneficial.
• Strong multitasking, project management, and execution abilities.
• Excellent interpersonal skills, including communication, presentation, persuasion, and influence.
• Effective organizational skills, demonstrating efficiency, punctuality, and collaboration in team settings.
• Proficiency in computer skills, including MS Office.

What Happens Next?

If you are interested in finding out more about this role please click the 'Apply' button. On submission of the job application form, an email alert is sent to the specialist consultant handling this role to register your interest.

All dialogue with us is in the strictest of confidence, without any obligation and we will NOT send your details to the relevant business without your consent.

Alternatively, to find out more about this role or any other roles that maybe relevant, you can email us at [email protected] or call our Medical Devices team on 01423 813456

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