Coordinador/a de Estudios Clinicos (CRC)
Core
Support clinical trial sites in all related activities according to ICH-GCP, protocol requirements, and study timelines.
Role type
Clinical Research Coordinator (CRC)
Builds
Clinical trial data and patient enrollment
Domain
Clinical research / Life Sciences
Required skills
ICH-GCP compliance, patient enrollment tracking, data entry in EDC systems, adverse event reporting, investigational product handling, regulatory document management, contract negotiation support, audit preparation
Preferred skills
Nephrology clinical studies experience
Technologies
EDC systems
Responsibilities
Act as main communication line between Sponsor/CRO and site; assist in scheduling monitoring visits; track patient enrollment; maintain study documents; enter data into EDC systems; report adverse events; handle investigational products; prepare for audits; support contract negotiations.
Seniority
Mid-level, hands-on IC