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Medical Director Mechelen Belgium,  

Galapagos (company)

Posted on : 11 May 2017

Project Description

As a medical director, you will participate in the development of the clinical development strategy and plan. 
You will be the responsible physician leading clinical studies for evaluation of new drug candidates in development.  
In particular, you will: 
  • Be a core member of the Clinical Development Team (CDT)
  • Bring the right medical and clinical development expertise to develop the Clinical Development Plan (CDP)
  • Play a leading role in designing and implementing specific studies of the CDP
  • Be the medical representative in clinical study teams
  • Lead or assist with Competent Authority and Ethics Committee/IRB submissions
  • Be the primary contact for medical review of safety information from clinical trials
  • Collaborate with the responsible person for safety reporting
  • Work closely with Clinical Operations to ensure
    • Adequate executions of Medical aspects of the study
    • Assessment of trial feasibility and investigator/site selection
    • Interaction with medical counterparts at CRO
  • Interact with key opinion leaders
  • Be the spokesperson on medical topics to external and internal bodies
  • Be compliant with GCP and other regulations  

Requirements for the successful candidate: 
  • MD or MD/PhD (relevant experience in Immunology and Inflammation preferred)
  • Has a strong scientific foundation with preferably work or post-doctoral training experience in an academic institution
  • 5 or more years of experience in clinical research
  • Solid understanding of Phase I  III drug development
  • 2 or more years of experience in the Pharmaceutical industry at Clinical Development Headquarters
  • Strong leadership skills and a strategic thinker
  • Energetic with a can-do attitude
  • Strong scientific and analytical skills
  • English speaking and writing skills are required  


Mechelen Belgium

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