Clinical Programming - SDTM
PharmaCRO
Job description
We are seeking highly experienced SDTM Programmer candidates with minimum 6 years of relevant experience CRF annotation Strong understanding of CDISC standards, including the SDTM Implementation Guide and regulatory authority submission guidelines Hands‑on experience in developing, validating, and reviewing SDTM domains Sound knowledge of submission deliverables, including P21, define.xml, and SDRG Strong programming skills, with advanced SAS expertise (Working knowledge of SQL and Python will be an added advantage) 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 IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
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