Clinical Research Associate I/II
Precision For Medicine
full-time
Posted on:
Location Type: Remote
Location: France
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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.
- Experience managing oncology studies
- Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions)
- Excellent communication and organizational skills are essential. A team player.
- Evidence of a client focused approach
- Fluency in English and for non-English speaking countries the local language of country where position based
Benefits
- Health insurance
- Flexible working hours
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical study monitoringregulatory submissionsprotocol adherenceSOPsICH-GCPoncology studiesdata recordingstudy initiationinvestigator identificationclinical research associate (CRA)
Soft skills
communication skillsorganizational skillsteam playerclient focused approach