Senior Clinical Research Associate
Core
Conducting onsite monitoring visits, driving study startup, and ensuring subject safety, rights, and data compliance for Phase II/III clinical trials.
Role type
Senior Clinical Research Associate (freelance/contractor)
Builds
Clinical trial data and regulatory submissions
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Independent on-site monitoring, CRF review, source document verification, query resolution, site management, feasibility research, regulatory document preparation
Preferred skills
Oncology study experience, Phase II/III trial experience
Technologies
MS Office
Responsibilities
Conducting and reporting onsite monitoring visits, driving study startup phase, performing CRF reviews and source document verification, managing site communication and schedules, supervising study timelines, acting as point of contact for support services and vendors, supporting quality control and compliance monitoring, participating in feasibility research, supporting regulatory team in study submissions
Seniority
Senior, hands-on IC