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Senior Statistical Programmer Fsp

6-8 years
Not Disclosed
10 April 4, 2025
Job Description
Job Type: Full Time Remote 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

 


Job Title:

Senior Statistical Programmer – FSP

Company:

Cytel

Location:

India (Remote)

Job Type:

Full-time


Job Summary:

As a Senior Statistical Programmer at Cytel, you will work sponsor-dedicated, fully embedded within one of Cytel’s global pharmaceutical clients. This is a fully remote position offering autonomy, innovation, and exposure to cutting-edge clinical research. You will lead or support Phase I–IV trials using your expertise in SAS programming and CDISC standards to deliver high-quality data outputs that support regulatory submissions and internal decision-making.


Key Responsibilities:

  • Perform data manipulation, analysis, and reporting of clinical trial data (safety and efficacy, including ISS/ISE) using SAS.

  • Generate and validate CDISC SDTM and ADaM datasets, and produce tables, listings, and figures (TLFs).

  • Conduct production and QC/validation programming tasks.

  • Generate complex ad-hoc reports using raw data.

  • Apply strong understanding of efficacy analysis.

  • Create and review submission documents, including eCRTs and define.xml.

  • Communicate with cross-functional teams and clients regarding specifications, project status, and data-related inquiries.

  • Act as lead programmer when required and manage multiple projects.

  • Adapt and respond to evolving project priorities and timelines.


Ideal Candidate Will Possess:

  • Education:

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

    • Master’s degree preferred.

  • Experience:

    • Minimum 8 years of SAS programming experience with clinical trial data (6 years with a Master’s).

    • Prior experience as a study lead programmer is preferred.

    • Experience supporting studies in immunology, respiratory, or oncology is a plus.

    • Familiarity with the clinical trial lifecycle and regulatory submission processes.

  • Skills:

    • Advanced SAS programming for data manipulation, reporting, and analysis.

    • Proficiency with CDISC standards (SDTM and ADaM).

    • Strong QC and validation expertise.

    • Solid ad-hoc reporting abilities.

    • Efficacy analysis experience is essential.

    • Excellent analytical and troubleshooting skills.

    • Strong communication skills for cross-functional and global teamwork.

    • Proven ability to meet deadlines with high-quality deliverables in a remote and collaborative environment.


Company Values at Cytel:

  • Scientific rigor

  • Intellectual curiosity

  • Collaboration and diversity of thought

  • Innovation and cutting-edge technology