Experienced Clinical Research Associate
Core
Conduct on-site clinical monitoring visits for research sites to ensure data integrity and regulatory compliance in medical trials.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial data and regulatory compliance for biotechnology and pharmaceutical clients
Domain
Clinical research / Biopharma
Deliverable
physical/clinical work
Required skills
Source document verification, Case report form review, Adverse event reporting, Study drug inventory management, Patient recruitment assessment, Regulatory document review
Preferred skills
Medical terminology knowledge, Clinical patient management, Drug therapy techniques
Technologies
Clinical trial management systems (implied by context)
Responsibilities
Conduct pre-study, initiation, monitoring, and closeout visits for research sites; Perform source document verification and case report form review; Perform regulatory document review; Conduct study drug inventory; Perform adverse event and serious adverse event reporting and follow-up; Assess patient recruitment and retention.
Seniority
Experienced, hands-on IC
