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Sr Statistical Programmer(Sdtm, Adam &Tlf)

5+ years
Not Disclosed
10 April 11, 2025
Job Description
Job Type: 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 (SDTM, ADaM & TLF)
Location: Home-Based, India (Asia Pacific)
Company: Syneos Health
Job ID: 25002567 


Job Overview:

As a Senior Statistical Programmer at Syneos Health, you’ll develop and validate programs to support clinical trial data analysis and reporting using SAS. You will work in collaboration with global teams to ensure accurate and timely deliverables in accordance with client and regulatory requirements.


Why Join Syneos Health?

  • 29,000 employees in 110 countries

  • Collaborate on projects supporting 94% of novel FDA-approved drugs

  • Strong focus on career growth, training, and mentorship

  • Total Self culture supporting diversity, authenticity, and well-being

  • Work that matters — impacting patients and health outcomes worldwide


Key Responsibilities:

  • Develop SAS programs for summary tables, data listings, graphs, and datasets (SDTM/ADaM)

  • Validate programs and resolve discrepancies with biostatisticians and programmers

  • Maintain project documentation and ensure inspection-readiness

  • Manage workload across multiple projects, timelines, and priorities

  • Develop dataset/output specifications and foresee programming issues

  • Lead and mentor junior programmers; provide project direction

  • Review and provide input on Statistical Analysis Plans (SAP), annotated CRFs, mock shells, etc.

  • Represent programming function in internal and sponsor meetings

  • Ensure SOP and regulatory guideline compliance (ICH, GCP, etc.)

  • Occasionally required to travel


Qualifications:

  • Bachelor’s degree in statistics, scientific, or related field (or equivalent experience)

  • 5+ years of experience in clinical SAS programming

  • Strong knowledge in:

    • Base SAS & SAS Macros

    • CDISC SDTM & ADaM standards

    • TLF (Tables, Listings, Figures) generation

  • Good to have: experience with R, GitLab, and clinical domain knowledge

  • Proficient in English (written and verbal)

  • Strong communication, documentation, and time management skills


Additional Information:

  • Responsibilities and qualifications listed may vary at the company’s discretion.

  • Role compliance with global equality, disability, and employment standards.

  • No employment contract implied by this description.