Clinical Research Associate II/I
Core
Conduct on-site monitoring visits, review case report forms, verify source documents, and manage clinical study sites in China.
Role type
Clinical Research Associate (Phase II/III)
Builds
Clinical studies in Oncology and other therapeutic areas
Domain
Life Sciences / Clinical Research
Deliverable
client delivery
Required skills
On-site monitoring, CRF review, source document verification, query resolution, site communication, feasibility research, regulatory document preparation, audit/inspection participation
Preferred skills
Oncology therapeutic area experience
Technologies
MS Office
Responsibilities
Conduct SSV, SIV, RMV, and COV onsite monitoring visits; Perform CRF review and source document verification; Resolve queries; Manage site communication; Support regulatory submissions; Participate in audits and inspections
Seniority
Mid-level, independent execution