Clinical Project Manager - CPM

Brussel

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2 Applied

Job description

  • Overall management of clinical studies (deadlines, budget, recruitment, SAE, etc.)
  • Organise investigator meetings
  • Coordinate CRO selection
  • Vendors management
  • Support the preparation of Clinical Trial Protocols
  • Prepare annual safety reports
  • Ensure the development of safety monitoring plans
  • Organise clinical meetings (manage agenda and minutes)

Benefits

  • Challenging projects based on your interests and skills
  • Personal follow-up and clear, transparent communication both before and after commencement of employment
  • Possibility to follow extra training
  • Inspiring network events and legendary after work drinks
  • Strong network of industry leading clients
  • Expertise within IT, Engineering and Life Sciences
  • A flying start for every junior, growth opportunities and possibility to share gathered knowledge for more senior employees

Have you got what it takes?

Apply
  • Bachelor or Master's degree in a scientific field
  • Minimum 5 years of experience in clinical research
  • Previous experience in Project Management preferred
  • Fluency in English is a must, French preferred, Dutch an asset
Reference number: 31730

Specifications

  • Nights
  • Weekends
  • Standby
  • Shifts
  • Employee
  • Freelance
Amandine Jansen
Recruitment Consultant
+32 491 15 34 75Mail me

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