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Lead CRA

02/08/2019
- Woluwe-Saint-Lambert

Intro

The position reports to the Head of Monitoring department. The Lead CRA is responsible to handle management of on-site monitoring activities.

Job content
  • Coordination of internal and/or external monitoring activities (i.e. monitoring reports review, advice on actions, tracking of visits schedule, monitoring documents, monitoring plan, monitoring budget)
  • Training and coaching of internal CRAs and external CRAs
  • Ensure the study CRA handover (internal CRAs)
  • Participate to the maintenance of the QA&C tracking tools
  • Provide assistance to the CRAs in the management of non-compliance issues
  • Ensure close collaboration between all actors of clinical trial research, as a privilege link between monitoring actors and the study team
  • Perform co-monitoring visits
  • Support in the Monitoring visits when required
  • Develop and maintain the procedures and templates related to monitoring activities
  • Escalate serious quality issues to Head of QA&C Unit
Profile
  • Master degree in life sciences
  • At least 3 years experience as CRA
  • Fluently in English. Dutch and French are a plus.
  • Problem solver
  • Great organisation and planning skills


What do we offer?

We offer you a challenging position in an competitive and dynamic culture with a market-compliant salary.

Contact

For more information contact Laura Schollen: laura@arcq or +32 16 30 95 09