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