Clinical Research Associate II
Core
Conduct onsite monitoring visits, study startup, and regulatory document preparation for Phase II/III clinical studies.
Role type
Clinical Research Associate II
Builds
Clinical studies in various therapeutic indications
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Onsite monitoring, CRF review, source document verification, query resolution, site communication, regulatory document preparation
Preferred skills
Study feasibility research, vendor management, internal project coordination
Technologies
MS Office
Responsibilities
Conduct and report onsite monitoring visits; Perform CRF review, source document verification, and query resolution; Support regulatory team in preparing documents for study submissions
Seniority
Mid-level IC
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