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IQVIA | Barcelona, Spain | Posted June 17, 2026
Position Overview
Responsible for delivery and/or may manage a team of employees responsible for executing site activation activities that may include:
Essential Functions
Site identification and feasibility activities, Regulatory, start-up, and maintenance activitiesPreparation, review, negotiation and management of site regulatory documentation and clinical trial agreements with sites and sponsorsMaintains, reviews, and reports on site activation performance metricsServes as the primary point of contact for investigative sites and/or sponsors;Ensures tracking completion of all regulatory and contractual documents for sitesEstablishes project timelines.Ensures all site activation activities are performed in accordance with all regulations, SOPs, Work Instructions and project requirements either at the global, regional, or country level and all relevant documents are submitted timely to the Trial Master File as pe...