Senior Clinical Research Associate

Senior Clinical Research Associate

Our client is seeking an experienced CRA II or Senior CRA with strong oncology experience to take full ownership of 1–2 clinical protocols. This role goes beyond traditional monitoring, encompassing contract negotiation, start‑up activities, monitoring, and close‑out responsibilities. You will operate with autonomy while being supported by a company culture focused on growth, wellbeing, and internal career progression.
Location:
Brussels, Belgium

• 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 race, sex, disability, religion/belief, sexual orientation, or age. We are an equal opportunities Recruitment Business and Agency.