Senior Clinical Research Associate
Core
Conduct on-site monitoring visits (SIV, RMV, COV), review case report forms, verify source documents, and resolve queries for Phase II/III clinical studies.
Role type
Senior Clinical Research Associate
Builds
Clinical trial data integrity and regulatory compliance for oncology and other therapeutic areas
Domain
Life Sciences / Clinical Research
Required skills
On-site monitoring, CRF review, source document verification, query resolution, site management, feasibility research, regulatory document preparation, audit/inspection participation
Preferred skills
Oncology experience
Technologies
MS Office
Responsibilities
Conduct and report SIV, RMV, COV onsite monitoring visits; Perform CRF review, source document verification and query resolution; Be responsible for site communication and management; Participate in feasibility research; Support regulatory team in preparing documents for study submissions; Prepare and participate on audits and inspections
Seniority
Senior, hands-on IC