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Clinical Research Associate 1
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Full-time
- Job Summary:Coordination of clinical research studies.
- Performance of regulatory tasks including IRB andsponsor/CRO regulatory correspondence.
- Pre-screen, Screen, and enroll research participants in outpatient and inpatient clinical trials.
- Schedule and conduct follow up research appointments for clinical trial participants.
- Data collection and entry into paper and electronic databases.
Expired 5 days agoInactive Job
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