Experienced Clinical Research Associate - Sign-On Bonus
Core
Conduct qualification, initiation, monitoring, and closeout visits for clinical research sites to ensure compliance with protocols and regulations.
Role type
Experienced Clinical Research Associate (IC)
Builds
Clinical trial data integrity and regulatory compliance for biotechnology, pharmaceutical, and medical device clients
Domain
Clinical Research / Life Sciences
Required skills
Clinical trial monitoring, GCP compliance, protocol deviation management, source data verification, adverse event reporting, site qualification, regulatory document review, patient recruitment assessment
Preferred skills
Experience in oncology, cardiology, or metabolic therapeutic areas
Technologies
Microsoft Office, Case Report Forms (CRF), Investigator Site Files (ISF)
Responsibilities
Conduct on-site monitoring visits; Verify investigator qualifications and resources; Review medical records and source documentation; Monitor adverse events and serious adverse events; Assess patient recruitment and retention; Complete monitoring reports and follow-up letters
Seniority
Mid-level, hands-on IC
