Position: Entry level

Job type: Full-time

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SENIOR CLINICAL RESEARCH ASSOCIATE – ANTWERPAs a Senior Clinical Research Associate (CRA), you will have the fantastic opportunity to join one of our CRO clients. This company are a global mid-sized CRO that strives to push boundaries by innovating and inventing. They are executing a high amount of studies globally and due to some late success with one of their Biotech clients they are looking for an experienced monitor.As a Senior Clinical Research Associate, a typical day might include the following:
  • Managing investigative site activities for multiple protocols / indications and providing ongoing updates of site status to the Study Manager / sponsor.
  • Creating and implementing subject enrolment strategies for assigned investigative sites.
  • Conducting study site visits (pre-study, initiation, monitoring, and close-out) and completing site visit deliverables within given timelines in the Monitoring Plan.
  • Ensuring proper storage, dispensation, and accountability of all investigational product(s) and trial-related material.
  • Marinating tracking records for assigned sites including tracking of subject status, subject case report form (CRF) retrieval / source document review (SCV), regulatory documents, and investigational product.
  • Participating in development of CRFs and other study related documents (source documents, subject worksheets, Monitoring Plan, etc).
This Role Might Be For You If
  • You have a life Science Degree
  • You have 1+ years independent monitoring
  • Are willing to travel when required
  • Have a full driving licence
  • Are fluent in English speaking, reading & writing
Benefits Include
  • Competitive salary
  • Sponsor-dedicated positions
  • Clear progression routes
  • Car allowance
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Deadline: 31-12-2025

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