Clinical Research Associate
Core
Conduct onsite monitoring visits, manage clinical study sites, and support regulatory submissions for clinical studies across various therapeutic indications. (via careerplan.io/jobs/744000153155529-clinical-research-associate-at-psi-cro)
Role type
Clinical Research Associate (CRA)
Builds
Clinical studies for pharmaceutical/biotech clients
Domain
Clinical Research / Life Sciences
Required skills
Onsite monitoring, Source document verification, CRF review, Query resolution, Site management, Feasibility research, Regulatory document preparation, Audit/inspection support
Preferred skills
Study startup support, Vendor management, Internal project coordination
Technologies
MS Office
Responsibilities
Conduct and report all types of onsite monitoring visits, Perform CRF review and source document verification, Support regulatory team in preparing documents for study submissions, Participate in audits and inspections, Communicate with internal project teams regarding study progress
Seniority
Entry-level to Mid-level, hands-on IC