Senior Clinical Research Associate (Argentina)
Core
Senior Clinical Research Associate managing complex clinical trials across Argentina, ensuring patient safety, data quality, and site compliance.
Role type
Senior IC clinical research associate (site management)
Builds
Clinical trial operations for biopharma clients
Domain
Healthcare / Clinical Research
Required skills
Clinical trial monitoring, site management, regulatory document preparation, informed consent verification, adverse event processing, data review, risk management, investigator relations, travel management
Preferred skills
Rare/complex therapeutic area monitoring, EDC/EHR experience, oncology experience, contract negotiation, formal presentation skills
Technologies
EDC systems, TMF, ISF, CRF
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; process Serious Adverse Events; review clinical data and resolve queries; mentor junior staff; travel up to 60% for site visits.
Seniority
Senior, hands-on IC (via careerplan.io/jobs/5984091004-senior-clinical-research-associate-argentina-at-precisionmedicinegroup)