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 Clinical Research Associate (CRA)
Builds
Clinical trial operations and data integrity for biopharma studies
Domain
Clinical Research / Biopharma
Required skills
Clinical trial monitoring, site management, regulatory document preparation, informed consent verification, adverse event reporting, data review, protocol deviation management, investigator relationship management, travel management
Preferred skills
Rare/complex therapeutic area monitoring, EDC/EHR monitoring, oncology experience, contract negotiation, formal presentation skills, process improvement
Technologies
EDC systems, TMF, ISF, GCP-compliant monitoring tools
Responsibilities
Conduct on-site and remote monitoring visits (pre-study, initiation, routine, close-out), manage site start-up and feasibility, verify informed consent processes, review and resolve data queries, process serious adverse events, maintain Investigator Site Files, mentor junior staff, attend investigator meetings, travel up to 60% of the time
Seniority
Senior, hands-on IC with mentorship responsibilities
