Sr. CRA 3, Brazil, IQVIA Biotech
Core
Independently manage and monitor clinical trial sites to ensure compliance with protocols, GCP, and ICH guidelines, supporting patient recruitment and data quality.
Role type
Senior Clinical Research Associate (Sr CRA 3)
Builds
Clinical trials for biotech sponsors
Domain
Biotechnology / Clinical Research
Deliverable
physical/clinical work
Required skills
Site monitoring, GCP/ICH compliance, Source documentation review, Data query resolution, Regulatory document management, Patient recruitment support, Protocol training
Preferred skills
Therapeutic area knowledge, Relationship building with investigative sites, Mentoring junior CRAs
Responsibilities
Conduct site qualification, initiation, routine, and closeout visits; Review source documentation and resolve data queries; Track study milestones and ensure regulatory document maintenance; Collaborate with cross-functional teams; Mentor junior CRAs
Seniority
Senior, hands-on IC
