Senior Clinical Research Associate
Core
Conducting onsite monitoring visits, reviewing clinical data, and ensuring subject safety and data compliance for Phase II and III clinical trials.
Role type
Senior Clinical Research Associate (freelance contractor)
Builds
Clinical trial data integrity and regulatory compliance for oncology and gastroenterology studies
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Independent on-site monitoring, CRF review, source document verification, query resolution, site management, timeline supervision, quality control reporting
Preferred skills
Oncology study support, Gastroenterology study support
Technologies
MS Office
Responsibilities
Conducting and reporting onsite monitoring visits, Performing CRF reviews and source document verification, Managing site communication and schedules, Supporting quality control and compliance monitoring
Seniority
Senior, hands-on IC