Senior Clinical Research Associate (Brazil)
Core
Senior Clinical Research Associate managing complex clinical trials across Brazil, ensuring patient safety, data quality, and site compliance.
Role type
Senior Clinical Research Associate (CRA) (via careerplan.io/jobs/6181080004-senior-clinical-research-associate-brazil-at-precisionmedicinegroup)
Builds
Clinical trial operations and data integrity for biopharma studies
Domain
Clinical Research / Biopharma
Required skills
Clinical trial monitoring, site management, regulatory document review, informed consent verification, adverse event processing, data review (EDC), protocol deviation management, investigator relations, travel management, mentoring junior staff
Preferred skills
Rare/complex therapeutic area monitoring, EDC/EHR experience, oncology experience, contract negotiation, study design support
Technologies
EDC systems, TMF, ISF, clinical trial management tools
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