Clinical Research Associate I/II
Precision Medicine Group
full-time
Posted on:
Location Type: Remote
Location: France
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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 (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
- Excellent communication and organizational skills are essential. A team player.
- 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 and for non-English speaking countries the local language of country where position based.
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical research associate (CRA)oncology studies managementregulatory submissionsstudy monitoringprotocol adherenceSOPsICH-GCPsite managementclinical study coordinationdata reporting
Soft skills
communication skillsorganizational skillsteam playerinterpersonal skillsproblem-solving skillsattention to detailtime managementadaptabilitycollaborationleadership