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Sr Statistical Programmer(Adam & Tlf)

Syneos Health
5+ years
Not Disclosed
Pune, India
1 June 5, 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

Senior Statistical Programmer (ADaM & TLF)

Location: Pune, India (Hybrid)
Job ID: 25109222
Experience Required: 5+ Years
Employment Type: Full-Time

About Syneos Health

Syneos Health is a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. The company partners with pharmaceutical, biotechnology, and healthcare organizations throughout the drug development and commercialization lifecycle, helping bring innovative therapies to patients worldwide.

With a global team of over 25,000 professionals, Syneos Health combines clinical, medical affairs, and commercial expertise to deliver impactful healthcare solutions.


Position Summary

We are seeking an experienced Senior Statistical Programmer (ADaM & TLF) to support clinical trial programming activities, including the development of ADaM datasets, Tables, Listings, and Figures (TLFs), and validation programming. The ideal candidate will possess strong expertise in SAS programming, CDISC standards, and statistical analysis deliverables within a clinical research environment.

The candidate will also provide technical leadership, oversee programming deliverables, and collaborate closely with Biostatistics, Data Management, and cross-functional study teams to ensure high-quality and regulatory-compliant outputs.


Key Responsibilities

Statistical Programming & Analysis

  • Develop and maintain SAS programs for:

    • CDISC ADaM dataset creation

    • Tables, Listings, and Figures (TLFs)

    • Derived datasets and analysis outputs

  • Generate statistical outputs according to Statistical Analysis Plans (SAPs), programming specifications, and sponsor requirements.

  • Perform validation programming and quality control checks to ensure accuracy and consistency of deliverables.

  • Resolve programming discrepancies in collaboration with Biostatisticians and project stakeholders.

Study Documentation & Compliance

  • Maintain complete and inspection-ready study documentation.

  • Prepare and manage programming specifications, validation plans, QC documentation, and related study files.

  • Ensure compliance with:

    • CDISC standards

    • ICH Guidelines

    • SOPs and Work Instructions

    • Regulatory requirements

Project Management

  • Manage multiple studies and programming activities simultaneously.

  • Estimate timelines and effort for study deliverables.

  • Monitor project progress and proactively identify potential risks and mitigation strategies.

  • Adapt priorities and workload to meet changing project requirements.

Technical Leadership

  • Act as Lead Statistical Programmer on assigned studies.

  • Review and provide feedback on:

    • Statistical Analysis Plans (SAPs)

    • Annotated CRFs (aCRFs)

    • Mock shells

    • Programming specifications

    • Database designs

  • Coordinate programming activities and monitor deliverables from junior programmers.

  • Ensure programming standards and best practices are followed across projects.

Stakeholder Collaboration

  • Participate in:

    • Sponsor meetings

    • Study kickoff meetings

    • Bid defense meetings

    • Internal project discussions

  • Communicate project status, risks, and timelines effectively to stakeholders.

  • Support cross-functional teams to achieve study objectives.

Mentoring & Knowledge Sharing

  • Mentor and train junior statistical programmers.

  • Review programming work and provide constructive feedback.

  • Develop and deliver training materials and technical sessions.

  • Contribute to process improvements and departmental initiatives.

Additional Responsibilities

  • Support study deliverable transfers and project transitions.

  • Perform other programming-related duties as assigned.

  • Minimal travel may be required.


Required Qualifications

Education

  • Bachelor's degree in Statistics, Mathematics, Computer Science, Life Sciences, Pharmacy, Biostatistics, or a related scientific discipline.

  • Equivalent combination of education and relevant programming experience may be considered.

Experience

  • Minimum 5+ years of Statistical Programming experience within the Clinical Research, Pharmaceutical, Biotechnology, or CRO industry.

  • Proven experience supporting Phase I–IV clinical trials.

Technical Skills

  • Strong proficiency in:

    • SAS Programming

    • Clinical Trial Data Analysis

    • Statistical Reporting

  • Extensive experience with:

    • CDISC ADaM Standards

    • Tables, Listings & Figures (TLF) Generation

    • Validation Programming

    • Clinical Data Structures

Preferred Skills

  • Experience with:

    • ISS (Integrated Summary of Safety)

    • ISE (Integrated Summary of Efficacy)

    • Pooled/Integrated Study Analyses

  • Knowledge of regulatory submission requirements.

Soft Skills

  • Strong analytical and problem-solving abilities.

  • Excellent written and verbal communication skills.

  • Ability to work independently and collaboratively in a global environment.

  • Strong organizational and time management skills.

  • Ability to manage multiple priorities under tight deadlines.