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Clinical Research Associate (CRA) Location: Ghent, Belgium (Hybrid – 1–2 days per week in office) Travel: Approx. 3–4 site visits per month (including occasional visits in The Netherlands) About the Role We are looking for an experienced Clinical Research Associate (CRA) to join the clinical team at one of our small CRO partners. Where they are a smaller company this is a much broader and dynamic role where you will be involved in feasibility, site selection, regulatory activities, contract negotiations, and monitoring from Site Initiation Visit (SIV) through to Close-Out Visit (COV). You will have the chance to collaborate with their exciting client base primarily consisting on small Biotech's working within the fields of oncology, neurology, dermatology, gastroenterology, and rheumatology. Key Responsibilities Conduct site selection, initiation, monitoring, and close-out visits for IMP trials , primarily Phase II and III . Collaborate with multiple vendors (IRT, central labs, etc.). Support feasibility assessments and regulatory submissions (CTIS experience is a plus). Maintain compliance with protocols and regulatory requirements. Requirements 2–3 years CRA experience with full monitoring responsibilities for Phase II and III trials . Dutch speaker, fluent in English, and conversational French. Willingness to work from the Ghent office at least once per week (preferably twice). Ability to travel internationally for site visits. Experience in oncology trials is a strong plus. Familiarity with rare disease trials is desirable but not required. What We Offer Competitive salary (please indicate your current package and expectations upon application). Attractive benefits including: Meal vouchers Company car Group insurance & hospitalization coverage (including dental and ambulatory)23 + 12 holidays for full-time employees Profit premium & cafeteria plan options Apply Now If you are passionate about clinical research and meet the above criteria, we’d love to hear from you Please submit your CV along with your current and expected compensation details.
