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Sas Programmer

Medpace
0-2 years
INR 4.5 LPA – 7 LPA
Navi Mumbai, India
1 June 18, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology

SAS Programmer

Department: Biostatistics & Clinical Data Sciences
Location: Navi Mumbai, India
Company: Medpace
Function: Clinical Development / Statistical Programming
Experience: Freshers to 2 Years
Education: B.Pharm, M.Pharm, B.Sc, M.Sc, Biostatistics, Mathematics, Health Informatics, Biotechnology, Life Sciences


Role Summary

The SAS Programmer is responsible for developing, validating, and maintaining statistical programming outputs used in clinical trials. The role supports clinical data management, biostatistics, and clinical operations teams through the creation of analysis datasets, tables, listings, figures, and data validation programs.

The position provides a foundation for a long-term career in Clinical SAS Programming, Statistical Programming, Biostatistics, and Clinical Data Sciences.


Key Responsibilities

1. Clinical SAS Programming

  • Develop SAS programs for:

    • Analysis Datasets (ADaM)

    • Tables

    • Listings

    • Figures (TLFs)

  • Create reusable SAS macros and utilities.

  • Validate programming outputs according to SOPs and regulatory standards.


2. Clinical Data Management Support

  • Program and maintain mapped clinical databases.

  • Perform data validation and discrepancy identification.

  • Support data cleaning activities.

  • Coordinate database updates and transfers.


3. Statistical Programming Activities

  • Generate statistical outputs for clinical studies.

  • Support biostatisticians in data analysis activities.

  • Perform quality checks and validation of statistical outputs.

  • Assist in preparation of interim and final study analyses.


4. Data Quality & Compliance

  • Ensure programming activities comply with:

    • ICH-GCP

    • CDISC Standards

    • Company SOPs

    • Regulatory Requirements

  • Maintain audit-ready documentation.


5. Cross-Functional Collaboration

Collaborate with:

  • Clinical Data Management

  • Biostatistics

  • Clinical Operations

  • Medical Writing

  • Statistical Programmers

  • Project Management Teams


6. Continuous Learning & Development

  • Develop expertise in:

    • Base SAS

    • Advanced SAS

    • CDISC

    • SDTM

    • ADaM

    • Clinical Trial Data Structures

  • Participate in internal training and certification programs.


Required Qualifications

Education

  • Bachelor's or Master's Degree in:

    • Mathematics

    • Statistics

    • Biostatistics

    • Pharmacy

    • Biotechnology

    • Life Sciences

    • Health Informatics


Preferred Certifications

  • SAS Base Certification

  • SAS Advanced Certification (Future)

  • CDISC Fundamentals