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Senior Statistical Programmer Fsp

8+ years
Not Disclosed
10 April 17, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Senior Statistical Programmer FSP

(India – Hybrid)

Job ID: 399
Job Category: Statistical Programming - FSP
Job Schedule: Full Time
Posting Date: April 14, 2025


Locations (Hybrid):

  • Pune – 5th Floor, Lohia-Jain IT Park, Maharashtra, 411038, IN

  • Hyderabad – Building 3A and 3B, Telangana, 500081, IN


Position Overview:

Sponsor-dedicated role fully embedded with a global pharmaceutical client. As a Senior Statistical Programmer, you will apply advanced SAS programming and CDISC standards expertise to support or lead Phase I–IV clinical trials. This hybrid role combines autonomy with innovation in a global setting.


Responsibilities:

  • Perform SAS-based data manipulation, analysis, and reporting (safety and efficacy)

  • Generate and validate SDTM & ADaM datasets, TLFs

  • QC/validation programming and complex ad-hoc report generation

  • Support efficacy analysis and create submission docs (define.xml, eCRTs)

  • Collaborate with cross-functional teams and communicate on project status

  • Step into a lead role when needed; adapt to shifting priorities


Qualifications:

  • Bachelor’s in Statistics, Computer Science, Mathematics, or related

  • 8+ years of SAS programming experience (or 6+ with a Master's) in pharma/biotech

  • Solid experience in CDISC SDTM & ADaM

  • Experience leading studies and managing multiple projects

  • Proficient in efficacy analysis and regulatory submission processes

  • Knowledge of the clinical development life cycle

  • Bonus: Experience in oncology, immunology, or respiratory studies

  • Excellent problem-solving, QC, and troubleshooting skills

  • Comfortable working in globally dispersed, multicultural teams


About Cytel:

Cytel is the world’s largest provider of statistical software and advanced analytics for clinical trials. With over 30 years of experience, Cytel supports global biotech and pharma companies in unlocking data value through scientific rigor and operational excellence. The company offers dynamic careers across biostatistics, statistical programming, AI, RWE, adaptive trials, and more—all while contributing to advancements in human health.