Job DescriptionProject Role: SAS Programmer
NWork Experience: 4+ Years
NWork location: Any IQVIA office Location In India
NWork Mode: Hybrid
NMust Have Skills: Clinical SAS/DM SAS/SAS Macros
NNote: this position is not for Statistical programming
NJob Description
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- Works collaboratively within Biometrics assisting in providing support to Clinical Data Management activities. N
- Works collaboratively with Statistical Programmer, Clinical Data Manager, Biostatistician, Global Drug Safety, Regulatory and Project Management staff and vendors to meet project deliverables and timelines for clinical data acquisition, quality checking and reporting. N
- Ensures completeness, correctness and consistency of clinical data and data structure. N
- Provides timely supportto the study team on all programming matters according to the project plan and programming specification using internal standards and guidelines. N
- Provides input on clinical data validation specifications and data transfer specifications. N




- Contributes to the reporting of routine clinical data through regulatory approval, product launch and annual reports. N
- Contributes to the monitoring of data quality during study conduct, providing information on issues along with proposed solutions. N
- Ensures completeness, correctness and consistency of clinical data and data structure. N
- Acts as Study Clinical Programmer N
- Reviews and accepts work by supporting Clinical Programmer N
- Attend Study Meeting Team to provide inputs as needed. N
- Provides guidance to timeline for deliverables. N
- Performs extract, map, transform, and load of clinical data. N
- Generates edit checks, listings and reports. N
- Performs study tasks. N

nRequires a minimumof Bachelor's degree in Mathematics (or equivalent) / Computer Science.
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- Excellent verbal and written communication skills and interpersonal skills are required. N
- Working understanding of pharmaceutical clinical develo

📌 Hiring: Sas Programmer (Bengaluru)
🏢 IQVIA India
📍 Bengaluru