Job Title: SAS + R Programmer
Location:
India (Remote)

Job Type:
Full-Time

Job Description
We are seeking an experienced
SAS + R Programmer
with strong clinical programming expertise to support clinical trials across multiple phases. The ideal candidate will have hands-on experience with
SAS programming, CDISC standards (SDTM/ADaM), TLF generation, and regulatory submissions
while working collaboratively with cross-functional clinical teams.

Key Responsibilities
- Develop, validate, and maintain SDTM and ADaM datasets in compliance with CDISC standards.
- Program and validate Tables, Listings, and Figures (TLFs) for clinical study reports.
- Review CRFs, SAPs, data specifications, and study documentation to ensure accurate programming.
- Perform quality control (QC) and ensure traceability throughout programming activities.
- Independently manage assigned clinical studies while meeting project timelines and quality standards.
- Troubleshoot data issues, resolve discrepancies, and deliver submission-ready outputs.
- Collaborate with biostatistics,



data management, medical writing, and project teams.
- Support process improvements, automation initiatives, and programming standards.
- Conduct peer reviews and mentor junior programmers when required.

Required Qualifications
- 5+ years of SAS programming experience in clinical trials.
- Strong expertise in SDTM, ADaM, TLF programming, CDISC standards, and regulatory submissions.
- Experience working on Phase I-IV clinical trials.
- Ability to manage multiple studies independently with minimal supervision.
- Solid analytical, problem-solving, and communication skills.
- Experience with global studies, FSP engagements, or regulatory submissions is a plus
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📌 SAS + R Programmer (India)
🏢 Trispoke Managed Services
📍 India