Project Specialist - Clinical Registry Coordinator - UK Based
On-siteReading, England, United Kingdom
Job Summary
Provide clinical registry support, oversight, and accountability for development programs by establishing expectations with internal and external partners. Submit approved documents to registries worldwide and track, report, and document disclosure records in group systems. Assist partners in maintaining accurate source data for the disclosure process and ensure timely resolution of planning issues for compliant delivery. Maintain accurate and correct data relevant to the disclosure process while ensuring all deliverables meet deadlines. This role supports the clinical development team within IQVIA's global clinical research services to accelerate innovative medical treatments and improve patient outcomes.
Required Qualifications
- A minimum of 4 years of relevant pharmaceutical/scientific experience in a clinical development environment (pharmaceutical, medical device, CRO, or other clinical development service organization)
- Bachelor's degree in Health or Science discipline
- experience in clinical research
- Clinical Registry experience preferred
- Experience working on a clinical trial or regulatory document management preferred
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