Clinical Research Associate (CRA) - Oncology - Clinical Operations

Excelya · Antwerp, Flanders, Belgium

You will continue to the employer’s original posting.

Company
Excelya
Location
Antwerp, Flanders, Belgium
Employment type
Full-time
Posted
June 5, 2026

About this job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. In this hands-on role, you will support site activation, documentation, regulatory submissions, and ensure TMF quality and inspection readiness. Working closely with cross-functional teams, you will help drive efficient study execution while maintaining full compliance with regulations and internal standards. Main Responsibilities: Coordinate site activation activities and ensure all essential study documentation is collected, reviewed, and filed Support the site “green-light” process prior to site initiation Organize and prepare Site Initiation Visits (SIVs) and ensure ISF r

This is a short summary. The full description is on the employer’s page.

Get matched to jobs like this

Create a free profile and receive vacancies from Belgium and across the EU that match your skills.

Get my matches