Clinical Research Associate I/ Clinical Research Associate II
Precision Medicine Group
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇳🇱 Netherlands
Visit company websiteJob Level
JuniorMid-Level
Tech Stack
Google Cloud Platform
About the role
- You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
- You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
Requirements
- Life science degree and / or equivalent experience
- 1 year 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.
- Experience managing oncology studies
- Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions)
Benefits
- Excellent communication and organizational skills are essential.
- Evidence of a client focused approach
- Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions)
- Fluency in English, Dutch and French.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical study monitoringregulatory submissionssite managementoncology studies managementICH-GCPSOPs complianceclinical researchdata recordingprotocol adherence
Soft skills
coordinationcommunicationorganizational skillsproblem-solvingattention to detail
Certifications
life science degree