Experienced Clinical Research Associate (remote-based)
Core
Conducting qualification, initiation, monitoring, and closeout visits for clinical research sites to ensure protocol compliance and data accuracy.
Role type
Experienced Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for biotechnology, pharmaceutical, and medical device clients
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Clinical trial monitoring, protocol adherence, source data verification, adverse event reporting, site qualification, regulatory document review, patient recruitment assessment
Preferred skills
Experience in oncology, cardiology, metabolic, endocrinology, CNS, or anti-viral/anti-infective therapeutic areas
Technologies
Microsoft Office
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits for research sites; Verify investigator qualifications, training, and resources; Review medical records and source documentation against CRF data; Verify eligibility of enrolled subjects; Review regulatory documents and manage drug/device inventory; Assess patient recruitment and retention success; Complete monitoring reports and follow-up letters.
Seniority
Mid-level, hands-on IC
