CRA2, IQVIA Biotech Argentina
Core
Clinical Research Associate conducting on-site monitoring of clinical trials in oncology, cardiovascular, or internal medicine.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for biotech sponsors
Domain
Life Sciences / Clinical Research
Deliverable
client delivery
Required skills
GCP, ICH guidelines, site monitoring, subject recruitment, protocol adherence, regulatory submissions, TMF/ISF management, data query resolution
Preferred skills
None stated
Technologies
None stated
Responsibilities
Conduct site visits (selection, initiation, monitoring, close-out); Collaborate on subject recruitment strategies; Deliver protocol training to site personnel; Assess site performance and escalate quality concerns; Monitor study progress (enrollment, CRF completion, data queries); Ensure document collection for TMF and ISF; Document site management activities; Support cross-functional project teams; Support site-level recruitment planning and financial management.
Seniority
Junior, hands-on IC
