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Statistical Programmer

Sun Pharma
Sun Pharma
2-12 years
Not Disclosed
Remote, India, India
1 May 8, 2026
Job Description
Job Type: Full Time Hybrid Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L.

Statistical Programmer Job | Remote/Hybrid | Sun Pharma

Company: Sun Pharmaceutical Industries Ltd.
Job Title: Statistical Programmer
Location: Remote / Hybrid
Job Type: Full-Time
Industry: Pharmaceutical / Clinical Research / Biostatistics / Clinical Data Programming


About Sun Pharma

Sun Pharmaceutical Industries Ltd. is one of the world’s leading specialty generic pharmaceutical companies, delivering high-quality medicines across global healthcare markets. The company operates across multiple therapeutic segments and focuses on innovation, clinical development, regulatory excellence, and patient-centric healthcare solutions.

Sun Pharma offers strong career development opportunities, global exposure, collaborative work culture, and advanced research environments for professionals in clinical research, biostatistics, data sciences, and regulatory operations.


Job Overview

Sun Pharma is hiring a Statistical Programmer to support programming activities across clinical development and regulatory submission projects. The selected candidate will lead and contribute to statistical programming tasks involving CDISC standards, SDTM/ADaM dataset creation, SAS programming, regulatory submissions, and clinical trial reporting.

The role requires expertise in clinical trial data programming, SAS development, regulatory submission support, and collaboration with global cross-functional clinical teams.

This opportunity is ideal for professionals experienced in clinical statistical programming, biostatistics, clinical data management, and regulatory submission programming within pharmaceutical, biotechnology, CRO, or healthcare organizations.


Experience Required

Experience Level

  • Mid-Level to Senior-Level Professional

Required Experience

  • Minimum 2–12+ years of experience in:
    • Statistical Programming
    • Clinical Trial Data Programming
    • SAS Programming
    • CDISC Standards Implementation
    • Regulatory Submission Programming

Preferred Industry Experience

  • Pharmaceutical Industry
  • Biotechnology Industry
  • CRO Industry
  • Clinical Research Organizations
  • Healthcare Data Analytics

Freshers are generally not eligible for this role.


Educational Qualification

Required Qualification

Candidates should possess a Bachelor’s degree or higher in:

  • Statistics
  • Computer Science
  • Mathematics
  • Engineering
  • Life Sciences
  • Related Disciplines