Clinical Research Associate - Entry
Core
Conduct on-site monitoring visits for clinical research sites to ensure compliance with protocols, GCP, and regulatory requirements for drug and medical device development.
Role type
Entry-level Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for pharmaceutical and medical device sponsors
Domain
Clinical Research / Biopharmaceuticals
Deliverable
physical/clinical work
Required skills
Site monitoring, regulatory document review, medical record verification, adverse event reporting, patient recruitment assessment, inventory management
Preferred skills
Health or life science background, familiarity with Microsoft Office, strong communication skills
Technologies
Microsoft Office
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits; Verify investigator qualifications and resources; Review regulatory documents and medical records; Verify subject eligibility; Report adverse events; Assess patient recruitment and retention; Complete monitoring reports.
Seniority
Entry-level, training-focused IC
