Clinical Trial Monitor I/ II
Core
Primary point of contact at the clinical trial site level responsible for study startup and overseeing site quality, integrity, and compliance.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial sites
Domain
Healthcare / Clinical Research
Required skills
Study startup, Quality oversight, Compliance monitoring, Protocol adherence, GCP knowledge, Regulatory requirements knowledge
Responsibilities
Study startup at site, Overseeing quality of clinical trial sites, Ensuring integrity of clinical trial sites, Ensuring compliance of clinical trial sites