Senior Clinical Research Associate 1 - Sponsor dedicated
Core
Conduct on-site monitoring visits (selection, initiation, close-out) to ensure data integrity and regulatory compliance for clinical trials.
Role type
Senior Clinical Research Associate (Sponsor-dedicated)
Builds
Clinical trial data and patient safety reports for life sciences clients
Domain
Clinical research / Life sciences
Deliverable
physical/clinical work
Required skills
On-site monitoring, GCP/ICH guidelines knowledge, subject recruitment planning, regulatory submission tracking, CRF completion management, data query resolution
Preferred skills
Therapeutic area knowledge, site collaboration
Technologies
MS Office
Responsibilities
Perform site selection, initiation, monitoring, and close-out visits; Support subject recruitment plan development; Evaluate site practices against GCP/ICH guidelines; Track regulatory submissions, recruitment, and data queries; Collaborate with study sites and client representatives
