Clinical Research Associate I/II
Precision Medicine Group
full-time
Posted on:
Location Type: Remote
Location: Romania
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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
- Not less than 6 months of experience 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.
- Oncology experience
- 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
- Competitive salary
- Remote work options
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical research associate (CRA)regulatory submissionssite managementclinical study monitoringICH-GCPSOPsclinical study protocoloncology experienceinvestigator identificationpre-study visits
Soft Skills
communication skillsorganizational skillsteam playerclient focused approach
Certifications
life science degree