Clinical Trials Governance Specialist
1 month ago
We are seeking a highly skilled Clinical Trials Governance Specialist to join our team at IQVIA. This exciting role will focus on providing expert-level support in coding governance and associated processes, ensuring the highest level of accuracy and reproducibility in clinical study data coding.
About the Role:- This is a full-time position offering a competitive salary of $85,000 - $110,000 per year, depending on experience.
- As a Clinical Trials Governance Specialist, you will be responsible for enabling the provision of consistent, accurate, and reproducible coding of clinical trial data, meeting individual project timelines.
- You will contribute to global thesaurus and code list maintenance, as well as maintaining and enhancing dictionary encoding products and systems.
- This role requires strong knowledge of industry standard coding thesauri (MedDRA, WHO Drug) and the ability to utilize and maintain incumbent dictionary encoding products and systems.
Key Responsibilities:
- Execute and promote adherence to established coding governance activities and principles.
- Contribute to delivery of consistent, accurate, and reproducible coding of clinical trial data meeting individual project timelines.
- Identify and report coding tools/systems issues to ensure tools/systems are consistently available for IDAR and external vendor users.
- Provide coding standards information and feedback to DM CRO vendor partners and all clinical teams.
- Understand and utilize encoding system functionality and tools to investigate system-related coding issues.
- Contribute to maintenance of coding process documentation.
About IQVIA:
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. Our mission is to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.
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