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Responsibilities
Ready to take your oncology experience to the next level with a global leader in clinical research? This is one you don’t want to miss 👇What you’ll be doing:Conducting site monitoring visits (initiation → close-out)Ensuring GCP / ICH compliance and protocol integrityActing as a key contact for sites - training, support & communicationTracking study progress: recruitment, CRFs, data queries, submissionsCollaborating with cross-functional study teams to drive executionWhat makes this role exciting?You’ll be at the frontline of oncological clinical trials — directly contributing to the development of innovative treatments that improve patient outcomes worldwide.Why IQVIA?Industry-leading innovation in clinical researchGlobal collaboration & career development opportunitiesExposure to cutting-edge technologiesBe part of a team improving patient access to life-saving treatments
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