Clinical Research Associate

Title: Clinical Research Associate

Client: Planet Pharma

• Lead and manage study start-up (SSU), including contract and budget negotiation.
• Perform independent on-site and remote monitoring visits (approx. 6–8 visits; flexible scheduling).
• Ensure site compliance with study protocols, GCP, and regulatory requirements.
• Manage study close-out activities and ensure delivery of high-quality data.
• Take full protocol ownership for typically two assigned studies.
• Collaborate cross-functionally with internal teams and site personnel.
• Maintain clear and timely study documentation and reporting.

• CRA II or Senior CRA level experience.
• Minimum 1.5 years of independent monitoring
  .
• Oncology experience required
  ;
  Phase I exposure strongly preferred.
• Fluency in French, Dutch, and English
  .
• Strong understanding of GCP and clinical research processes.
• Ability to work independently while managing multiple responsibilities.

Interested? Apply now for immediate consideration or contact Maria Tsalpatourou at mt

We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.