Clinical Research Associate I/Clinical Research Associate II
Precision Medicine Group
full-time
Posted on:
Location Type: Remote
Location: Italy
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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 and all applicable regulations
- Coordinate all necessary activities required to set up and monitor a study
Requirements
- Life science degree and / or equivalent experience
- At least 6 months experience as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent
- Experience managing oncology studies
- Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment
- Fluency in English and Italian
Benefits
- Competitive salary
- Remote work
- Professional development opportunities
- Health insurance
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical study monitoringprotocol compliancedata recordingreportingoncology studies managementlife science degreeCRO experiencepharmaceutical industry experiencebiotech industry experience
Soft Skills
organizational skillscommunication skillsinterpersonal skillsattention to detailproblem-solving skills