Senior Clinical Research Associate
Core
Oversees clinical monitoring and site management to ensure protocol adherence, data accuracy, and regulatory compliance for clinical trials.
Role type
Senior Clinical Research Associate (IC)
Builds
Clinical trial data and site compliance for sponsors and research organizations
Domain
Clinical research / Life sciences
Deliverable
physical/clinical work
Required skills
Clinical monitoring, site management, protocol adherence, data verification, regulatory compliance (GCP/ICH), training and mentoring, action item tracking, study document review, therapeutic area knowledge
Preferred skills
Complex study experience, leadership, process improvement, stakeholder engagement
Technologies
EDC systems, MS Office
Responsibilities
Conduct on-site and remote monitoring visits (SIV, routine, close-out); verify source data and CRFs for accuracy; manage site feasibility and selection; review safety events and protocol deviations; train and mentor site staff and junior CRAs; track and close action items; support investigator meetings.
Seniority
Senior, hands-on IC with mentorship responsibilities
