Clinical Research Associate I/II
Precision Medicine Group
full-time
Posted on:
Location Type: Remote
Location: Belgium
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Tech Stack
About the role
- Monitor and own the progress of clinical studies at investigative sites
- Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards
- Coordinate all necessary activities required to set up and monitor a study
Requirements
- Life science degree and / or equivalent experience
- 2 years or more as a CRA in either 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, as required
- Excellent communication and organizational skills are essential. A team player.
- Evidence of a client focused approach
- Fluency in English, Dutch
- French will be a plus
- Oncology monitoring experience will be a plus
Benefits
- flexible working arrangements
- professional development opportunities
- reasonable travel commitments
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical research associatemonitoring clinical studiessite managementICH-GCPSOPsregulatory complianceoncology monitoring
Soft Skills
communication skillsorganizational skillsteam playerclient focused approach
Certifications
life science degree