Clinical Research Associate II
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Job Description
Clinical Research Associate monitoring clinical trials in Belgium for a life-sciences CRO. Ensuring compliant site execution, study progress, regulatory submissions, and risk mitigation.
Responsibilities:
- Monitor and own the progress of clinical studies at investigative sites
- Ensure clinical studies are conducted, recorded, and reported according to protocol, SOPs, ICH-GCP, applicable regulations, and standards
- Coordinate activities required to set up and monitor studies
- Identify investigators
- Help prepare regulatory submissions
- Conduct pre-study and initiation visits
- Monitor sites in Belgium and occasionally support sites in the Netherlands
- Identify potential study risks and propose mitigation solutions
- Prepare for investigator meetings, site visits, and project team updates
Requirements:
- Life science degree and/or equivalent experience
- At least 2 years of experience as a CRA in a CRO or pharmaceutical/biotech industry, or equivalent relevant experience and/or demonstrated competencies
- Site management or equivalent experience in clinical research
- Availability for domestic travel including overnight stays
- Availability for approximately 50–60% travel commitment
- Excellent communication and organizational skills
- Team-player mindset
- Client-focused approach
- Fluency in English and Dutch
Benefits:
- Remote-based position
- Reasonable travel and improved work/life balance
- Lower than average number of protocols
- Support from direct line management
- Opportunity for influence and impact in a smaller CRO
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