Experienced Clinical Research Associate
Core
Full-time, home-based Clinical Research Associate supporting drug development from feasibility to closeout for Phase 1-3 trials.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial monitoring and data integrity for biotechnology, pharmaceutical, and medical device clients
Domain
Clinical Research / Drug Development
Deliverable
physical/clinical work
Required skills
Feasibility study execution, Source document verification, Case report form review, Regulatory document review, Study drug inventory management, Adverse event reporting, Patient recruitment and retention assessment
Preferred skills
Registered Nursing background, Dietician background, Pharmacy Technician background, Pharmaceutical Sales experience
Technologies
Clinical trial management systems (implied via source document/CRF review)
Responsibilities
Conduct feasibility, 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
Mid-level, hands-on IC
