Clinical Research Associate 2 – Multisponsor – South of Spain
Core
Conduct independent site monitoring, selection, initiation, and close-out visits for clinical trials to ensure protocol adherence and data integrity.
Role type
Clinical Research Associate 2 (Multisponsor)
Builds
Clinical trial data and regulatory compliance for pharmaceutical clients
Domain
Clinical Research / Pharmaceutical Trials
Deliverable
client delivery
Required skills
Independent site monitoring, GCP/ICH guidelines knowledge, therapeutic area knowledge, protocol administration, recruitment tracking, CRF management, data query resolution, regulatory submission tracking
Preferred skills
None stated
Technologies
None stated
Responsibilities
Perform site selection, initiation, monitoring, and close-out visits; Administer protocol training to sites; Evaluate site practices for regulatory adherence; Manage study progress including recruitment, CRF completion, and data queries; Maintain site management documentation
Seniority
Mid-level (2-4 years experience)
