Freelance Senior Clinical Research Associate
Core
Conducting onsite monitoring visits, reviewing clinical data, and managing clinical sites to ensure subject safety, data quality, and project timelines.
Role type
Senior Clinical Research Associate (Freelance/Contractor)
Builds
Clinical trial data integrity and site compliance
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Onsite monitoring, CRF review, source document verification, query resolution, site management, schedule supervision, quality control reporting
Preferred skills
Phase II/III trial experience, Oncology/Hematology/Infectious disease therapeutic areas
Technologies
MS Office
Responsibilities
Conducting and reporting onsite monitoring visits, performing CRF reviews and source document verification, managing site communication, supervising study timelines and schedules, acting as a point of contact for support services and vendors, supporting quality control and compliance monitoring
Seniority
Senior, hands-on IC
