Senior Clinical Research Associate 1 - Sponsor dedicated
Core
Conducting site selection, initiation, monitoring, and close-out visits for clinical trials to ensure data integrity and regulatory compliance.
Role type
Senior Clinical Research Associate (Sponsor-dedicated)
Builds
Clinical trial data and patient recruitment plans
Domain
Life sciences / Clinical research
Deliverable
client delivery
Required skills
Site monitoring, regulatory compliance (GCP/ICH), subject recruitment planning, data query resolution, travel management
Preferred skills
Therapeutic area knowledge, MS Office proficiency
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
Seniority
Mid-level, hands-on IC