Senior Clinical Research Associate
Core
Conduct on-site monitoring visits (SIV, RMV, COV) for Phase II/III clinical studies in various therapeutic indications, ensuring data quality and regulatory compliance.
Role type
Senior Clinical Research Associate (IC)
Builds
Clinical study data integrity and regulatory submission readiness
Domain
Clinical Research / Life Sciences
Required skills
On-site monitoring, CRF review, source document verification, query resolution, site management, feasibility research, audit/inspection preparation
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; Manage site communication and act as point of contact for support services and vendors; Communicate with internal project teams regarding study progress; Participate in feasibility research; Support regulatory team in preparing documents for study submissions; Prepare and participate in audits and inspections