Senior Medical Director

☞ argenx

Aussicht: 130

Update Tag: 26-11-2025

Ort: Ghent East Flanders

Kategorie: Gesundheit / Medizinische Versorgung

Industrie:

Position: Director

Jobtyp: Full-time

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Jobinhalt

For the expansion of our clinical team, argenx is looking for a Senior Medical Director.. This position provides strategic leadership and tactical oversight for the clinical/medical aspects of all phases of the clinical drug development process. The Senior Medical Director is responsible for the design, development and execution of Clinical Development Plans (CDPs), clinical trials and protocols in accordance with applicable GCP regulations. This person leads and contributes to the analysis of study results, the assessment of the extent to which the study(ies) has achieved clinical/regulatory objectives and the documentation of study results.

The Senior Medical Director may act as a clinical/medical representative in meetings with external stakeholders (e.g. collaborators, Key Opinion Leaders (KOLs), investigators, regulatory authorities, etc.), partners (e.g. vendors, consultants, etc.) and other external audiences as needed.

Key Accountabilities/Responsibilities

The position will have the following key responsibilities:
  • Provide medical content and leadership of the clinical studies
  • Medical Monitoring of clinical studies
  • Establish and approve scientific methods underlying the design and implementation of clinical protocols
  • Ensure study subject safety
  • Regularly review adverse event, laboratory and other clinical data, ensure reporting is done on a timely basis
  • Collaborate with the study executive and independent safety committee when needed
  • Represent clinical research through membership on trial teams.
  • Contribute to, review and approve study protocols, protocol amendments, study manuals, Investigator Brochures (IBs), Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs) and other clinical documents as required for the conduct of clinical trials
  • Interpret, summarize and document clinical data for regulatory documents (e.g. INDs, Annual Reports, NDAs, MAAs, etc.), manuscripts, and other publications as required.
  • Collaborate with leading academic medical centres
  • Recruit, guide and motivate clinical investigators
  • Ensure study compliance by understanding and applying all relevant SOPs and GCPs
  • Participate in long range strategic planning
Desired Skills And Experience
  • Demonstration and commitment to vigilant proactive problem solving
  • Excellent leadership abilities
  • Able to provide multiple examples of creating and implementing the scientific and clinical principles used for the preparation of clinical studies and clinical trial protocols.
  • Demonstrated expertise in clinical trial design, conduct and interpretation of clinical data.
  • Previous experience with regulatory submissions.
  • Excellent written and verbal communication skills.
  • Ability to travel.
  • MD degree, a minimum of 5 years of clinical drug development experience
  • Desirable: Experience in the therapy areas of (Monoclonal Antibodies) and/or Translational Medicine.
Offer
  • A competitive salary package with benefits;
  • A work environment in a human-sized, dynamic, rapidly growing biotech company
Job Info
  • Type: Full time
  • Location: Europe - Remote, Gent
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Frist: 10-01-2026

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