SrCRA, IQVIA Biotech Argentina
Core
Perform site monitoring and management to ensure clinical studies are conducted per protocol and regulations, focusing on oncology.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial data and patient access to oncology treatments
Domain
Life sciences / Oncology
Required skills
Site monitoring, subject recruitment management, protocol adherence, regulatory compliance, TMF/ISF management, data query resolution, site training
Preferred skills
Oncology therapeutic area experience, financial management of clinical trials
Technologies
Trial Master File (TMF), Investigator's Site File (ISF), Case Report Forms (CRF)
Responsibilities
Conduct site monitoring visits (selection, initiation, monitoring, close-out), drive subject recruitment plans, evaluate site quality and regulatory adherence, track study progress (submissions, enrollment, CRF completion), maintain site documentation, liaise with study teams
Seniority
Senior, hands-on IC
