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Medical Affairs Consultant – Waterloo, Belgium

Alsinova · Waterloo

Mid 🇬🇧 English
PowerPoint Word

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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Published 3 maanden geleden

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Alsinova

Waterloo