Clinical Research Associate II
Precision For Medicine
full-time
Posted on:
Location Type: Remote
Location: Hungary
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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
- 2 years or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent
- Availability for domestic travel including overnight stays, as required
- Excellent communication and organizational skills are essential. A team player.
- Evidence of a client focused approach
- Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment
- Fluency in English and Hungarian
- oncology monitoring experience will be a plus
Benefits
- reasonable travel
- work/life balance
- influence and impact during clinical trials
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical study monitoringregulatory submissionsICH-GCPSOPsprotocol complianceoncology monitoring
Soft Skills
communication skillsorganizational skillsteam playerclient focused approach