Clinical Research Associate II
Core
Conduct on-site clinical monitoring visits, support study startup, and ensure clinical research quality across Phase II/III trials.
Role type
Clinical Research Associate II
Builds
Clinical trial data integrity and regulatory submission documentation
Domain
Life Sciences / Clinical Research
Required skills
on-site clinical monitoring, source document verification, CRF review, clinical data query resolution, study startup support, feasibility research, regulatory documentation preparation, site relationship management, travel management
Preferred skills
oncology experience
Technologies
Microsoft Office
Responsibilities
Conduct and document on-site clinical monitoring visits; Participate in study startup and feasibility research; Perform CRF reviews and source document verification; Manage site communications and relationships; Collaborate with regulatory teams for submission documentation; Support consistent execution of clinical research activities
Seniority
Mid-level, hands-on IC