Virtual CRA Info Session - 11.4.2026 (Clinical Research Coordinator Experience)
Core
Conduct on-site and virtual monitoring visits at clinical research sites to ensure protocol compliance, data accuracy, and patient safety for biopharma and medical device trials.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial monitoring and compliance for biotechnology, pharmaceutical, and medical device companies
Domain
Clinical Research / Contract Research Organization (CRO)
Deliverable
client delivery
Required skills
Clinical Research Coordinator experience, site monitoring, regulatory compliance (GCP/SOPs), data verification, adverse event reporting, patient recruitment assessment
Preferred skills
Risk-based monitoring, centralized data review, therapeutic area expertise
Technologies
Integrated Clinical Trial Management System, Microsoft Office
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits; Verify investigator qualifications and resources; Review medical records and source documentation against case report forms; Monitor adverse events and investigational product accountability; Assess site patient recruitment and retention; Complete monitoring reports and follow-up letters
Seniority
Mid-level IC (requires 2+ years prior experience)
