Job Description
As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.
You will:
Conduct and report all types of onsite monitoring visitsBe involved in study startupPerform CRF review, source document verification and query resolutionFacilitate site budgets and contract negotiationsBe responsible for site communication and managementBe a point of contact for in-house support services and vendorsCommunicate with internal project teams regarding study progressParticipate in feasibility researchParticipate in quality control and compliance monitoringSupport regulatory team in preparing documents for study submissionsQualifications
College/University degree in Life Sciences, Pharma...