Global Data Manager - homebased (FSP)

Role overview

This position focuses on providing end-to-end data management support, oversight, and accountability across one or more clinical trials. The role involves working closely with trial customers and internal/external stakeholders to align expectations, manage deliverables, and maintain high-quality clinical data processes.

Key duties

• Act as the primary point of contact with trial customers and relevant partners to define and confirm data management expectations.
• Plan, coordinate, and monitor the content, format, quality, and timing of key data management outputs such as CRFs, data review plans, QC plans, oversight plans, database release plans, final datasets, submission packages, and archival materials.
• Collect integration needs and content requirements for eCRFs and other data capture tools together with the customer and functional teams.
• Define conventions and quality standards for clinical data and dataset structure.
• Set timelines for data management activities and follow through to keep milestones on track.
• Carry out study-level oversight activities in line with the oversight plan, QC process, and work instructions, with limited direction from the Data Management Lead.
• Prepare clinical data management documents, including submission packages, ensuring they are accurate, well-organized, scientifically sound, compliant, and consistent with regulatory and documentation standards.
• Maintain audit and inspection readiness for all trial data management deliverables and support regulatory inspections and audits when required.
• Support planning and tracking of all core data management deliverables to ensure timely completion.
• Contribute to assigned clinical working groups so that data management and therapeutic area requirements are met.
• Capture and share lessons learned, best practices, and common questions at trial level.
• Present information and deliver training during investigator meetings and monitor meetings.

Experience and qualifications

• A bachelor’s degree or higher, ideally in Health Sciences, or another bachelor’s degree or higher supported by professional clinical exposure.
• At least 5 years of experience in data management.
• Minimum 3 years in a lead or co-lead capacity.
• Previous experience managing vendors.
• Hands-on experience with RAVE.

Additional information

This position is not eligible for UK visa sponsorship.

Company overview

IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare sectors. The organization focuses on enabling the development and commercialization of medical treatments that improve patient outcomes and population health worldwide.

Hiring integrity

The company follows a strict integrity policy in recruitment and does not tolerate fraudulent applications. All details and credentials submitted must be accurate and complete. Any false information, misrepresentation, or material omission may lead to rejection of the application or termination of employment, subject to applicable law.