Key Responsibilities:Collaborate with business users to consolidate and document requirements for DH capabilities.Support planning and execution of validation and qualification processes for supplier systems.Write and execute detailed test scripts with precision and accuracy.Review and contribute to System Development Lifecycle (SDLC) documentation, including supplier release notes and change memos.Engage with stakeholders across privacy, security, quality, and regulatory functions.Participate in audits and inspections, fulfilling documentation and data requests.Support data standardization, integration, and ingestion across the DH landscape.Oversee supplier systems, managing issues, risks, and escalations as needed.Ensure compliance with internal processes and external regulatory requirements.Required Qualifications:Previous experience working in the CRO, Healthcare or Pharmaceutical IndustryExperience inComputer System Validation (CSV)andaudit/inspection participation.Familiarity withSoftware Development Life Cycle (SDLC)andGAMP5 methodology.Strong understanding ofClinical Trial SaaS platforms/applications.Excellentdocumentation,analytical thinking, andproblem-solvingskills.Ability to manage and communicate with multiple stakeholders effectively.Detail-oriented with a strong focus on process and activity execution.Preferred Experience:Knowledge of systems used bypreferred or established suppliersin the clinical trial space.Experience supportingsystem integrationsandchange controlprocesses.Exposure todata governanceanddigital health data ecosystems.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com