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 SIV, RMV, COV onsite monitoring visitsPerform CRF review, source document verification and query resolutionBe 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 researchSupport regulatory team in preparing documents for study submissionsPrepare and particiapte on audits and inspectionsQualifications
College/University degree in Life Sciences or an equivalent combination of education, training & experienceIndependent on-site monitoring experience<...