Clinical Research Associate (various Levels)
Core
Conducting on-site monitoring visits to ensure clinical trial data integrity and regulatory compliance for pharmaceutical studies.
Role type
Senior Clinical Research Associate (Sponsor-dedicated)
Builds
Clinical trial data and regulatory submissions for life sciences clients
Domain
Clinical research / Life sciences
Deliverable
client delivery
Required skills
On-site monitoring, GCP/ICH guidelines knowledge, subject recruitment planning, data query resolution, regulatory submission tracking
Preferred skills
Therapeutic area knowledge, flexible travel, driver's license
Technologies
MS Office
Responsibilities
Performing site selection, initiation, monitoring, and close-out visits; Supporting subject recruitment plan development; Evaluating site practices against GCP/ICH guidelines; Managing progress via tracking submissions, recruitment, CRF completion, and data queries; Collaborating with study sites and client representatives