Senior Clinical Research Associate (Chile)
Core
Senior Clinical Research Associate managing complex clinical trials, site start-up, on-site monitoring, and data quality for studies in Chile.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial operations and data integrity for pharmaceutical/biotech studies
Domain
Clinical Research / Biopharma (via careerplan.io/jobs/6181034004-senior-clinical-research-associate-chile-at-precisionmedicinegroup)
Required skills
Clinical trial monitoring, site management, regulatory document review, informed consent verification, adverse event reporting, data review (EDC/CRF), protocol deviation management, investigator relationship management, travel management, GCP/ICH-GCP compliance
Preferred skills
Rare/complex therapeutic area monitoring, EDC/EHR monitoring, oncology experience, contract negotiation, formal presentation skills
Technologies
EDC systems, TMF, ISF, tracking systems
Responsibilities
Conduct on-site and remote monitoring visits (pre-study, initiation, routine, close-out); manage site start-up including feasibility, recruitment, and regulatory submissions; verify informed consent and patient safety; review clinical data and resolve queries; process Serious Adverse Events; mentor junior staff; travel up to 60% for site visits.
Seniority
Senior, hands-on IC