Virtual Event: From Clinical Research Coordinator to CRA
Core
Conducting qualification, initiation, monitoring, and closeout visits for clinical research sites to ensure compliance with protocols and regulations.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for pharmaceutical and medical device development
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Clinical trial monitoring, regulatory compliance (GCP/SOPs), site qualification, source data verification, adverse event reporting, patient recruitment assessment, cross-functional collaboration
Preferred skills
Medical or life science background, travel readiness (60-70%), driver's license
Technologies
Microsoft Office
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