PHARMAFull-time
Clinical Programming - SDTM
BANGALORE (IN)ONSITEPOSTED: 8/12/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
ROLE DEFINITION & RESPONSIBILITIES
Perform Case Report Form (CRF) annotation according to CDISC SDTM standards and project guidelines.
Develop, validate, and review SDTM domains to support regulatory submission packages.
Ensure full compliance with CDISC SDTM Implementation Guides and regulatory submission requirements.
Generate and validate standard submission deliverables, including Pinnacle 21 (P21) reports, define.xml, and Study Data Reviewer's Guides (SDRG).
Utilize advanced SAS programming techniques to process, transform, and map clinical trial data.
REQUIRED VERIFIED SKILLS
CDISC SDTM
SAS
CRF Annotation
Pinnacle 21
define.xml
SDRG
Regulatory Submissions
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
ORGANIZATION CONTEXT & CULTURE
IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services (CRO) to the life sciences industry. The company helps pharmaceutical, biotech, and medical device clients accelerate the development and commercialization of new medical treatments through its extensive data, technology, and human expertise. Their offerings span from clinical trial design and execution to real-world evidence and commercial effectiveness.
TEAM SIZE: 87,000+ employees
INDUSTRY: Healthcare Technology & Contract Research
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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