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As a Clinical Data Coder at IQVIA, you will play a pivotal role in managing single and multi-service projects. Your expertise will ensure quality deliverables are met on time, within budget, and to the customer's satisfaction. You will provide leadership to the team in coding, project planning, execution, financial management, communication, and milestone tracking.
Responsibilities:
- Collaborate with the Study Data Manager to develop coding guidelines aligned with study requirements.
- Deliver timely, consistent, accurate, and reproducible coding using MedDRA and WhoDrug dictionaries.
- Perform independent quality control of coded data.
- Maintain coding setup UAT.
- Coordinate study timelines and manage workload.
Key Qualifications:
- Bachelor's degree in Pharmacy, dental, medical, nursing, life sciences, or a related field.
- At least 7 years of experience in clinical trials, including proven competence in managing coding and/or other data management processes for multiple global projects.
- Excellent knowledge of Medical Dictionaries used for coding.
- Strong understanding of the clinical drug development process.