Senior CRA - IQVIA Biotech
Core
Senior Clinical Research Associate performing on-site monitoring visits for oncology clinical trials to ensure GCP/ICH compliance and study integrity.
Role type
Senior IC Clinical Research Associate (Oncology)
Builds
Clinical trial data and regulatory compliance for biotech/pharma partners
Domain
Biotechnology / Clinical Research / Oncology
Required skills
On-site monitoring, Oncology therapeutic knowledge, GCP/ICH guidelines, Subject recruitment management, Protocol administration, TMF/ISF management, Data query resolution, Site financial management
Preferred skills
Bachelor's degree in scientific discipline or healthcare, English fluency, Microsoft Office proficiency
Responsibilities
Perform site monitoring visits (selection, initiation, monitoring, close-out), Drive subject recruitment plans, Administer protocol training to sites, Evaluate site quality and adherence to regulations, Manage study progress (submissions, enrollment, CRF completion), Maintain Trial Master File and Investigator's Site File, Generate visit reports and action plans, Support site financial management
Seniority
Senior, hands-on IC
