28 set - Bardi
Iqvia
In this role, you support feasibility, site identification, regulatory, start-up, and maintenance activities at regional or country levels. You work as a SPOC with the Site Activation Manager and cross-functional teams to ensure documents, timelines, and contracts are properly managed. You will prepare and review site documentation and maintain project systems to track progress and compliance. You contribute to site activation by coordinating regulatory, ethics, and ICF-related activities while upholding SOPs and contractual guidelines. This position offers exposure to a global clinical research environment that aims to improve patient outcomes and population health.Serve as a single point of contact for feasibility, site activation, and some maintenance activities in assigned studiesReview site documents for completeness, consistency, and accuracy under supervisionPrepare and review site documentation and notify team upon completionDistribute completed documents to sites and internal stakeholdersMaintain internal systems, databases, tracking tools, timelines,
and project plans with accurate dataTrack and follow up on progress, approvals, and execution of regulatory, ethics, CDAs, ICF, and IP release documentsAssist in updating contracts and ensuring full executionCoordinate with SAM, Project Management, and other departments to support site activation at country/region levelMonitor and report on site performance metricsEnsure adherence to local and international regulations and SOPsBachelor's degree xysqume in Life sciences or related field1–3 years’ clinical research or relevant experienceAlternatively 3 years’ experience in a healthcare environment or equivalentRegulatory and ethics documentation experience (ICF, CDAs, IP release)Strong attention to detail and documentation managementCross-functional collaborationGood communicationRegulatory documentation managementContract review and trackingProject tracking tools and databases#J-18808-Ljbffr
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