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Senior / Principal Stat Programmer(Sas/ R, Sql)

5+ years
Not Disclosed
10 Sept. 19, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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 / Principal Stat Programmer (SAS / R, SQL)

Updated: September 12, 2025
Location: IND – Gurugram – Hybrid
Job ID: 25101677


About Syneos Health

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.

  • Present in 110 countries with 29,000+ employees.

  • Partnered with 94% of FDA-approved drugs and 95% of EMA-authorized products over the last 5 years.

  • Delivered 200+ studies across 73,000 sites and 675,000+ trial patients.

We are committed to a Total Self culture, diversity, inclusion, and employee well-being while simplifying processes to enhance both client and employee experience.

Work Here Matters Everywhere.


Why Join Us

  • Career development & progression opportunities.

  • Supportive and engaged line management.

  • Technical and therapeutic training.

  • Peer recognition programs & total rewards.

  • Culture of authenticity, inclusion, and belonging.


Key Responsibilities

  • Develop programs and provide statistical programming support for statisticians, clients, or business needs.

  • Source, organize, and interpret complex datasets.

  • Create statistical tables, listings, and graphs.

  • Develop codes for analysis datasets, tables, and figures.

  • Evaluate programming processes and suggest improvements for productivity.

  • Manage or contribute to cross-functional projects, programs, or processes.

  • Direct and mentor junior-level professionals.

  • Contribute to the design, implementation, and delivery of statistical programming processes and policies.


Required Skills & Qualifications

  • 5+ years’ experience in Advanced SAS / R programming and SQL.

  • Strong expertise in R programming and R package development.

  • Knowledge of Python (preferred, value-added).

  • Experience with TIBCO Spotfire (or similar tools) including calculated columns, markings, filtering, and document properties.

  • Strong understanding of clinical domain and drug development process (Phases I–IV).

  • Experience in Clinical Data Management.

  • Prior study lead experience; ability to manage multiple studies.

  • Excellent written and verbal communication skills.


Role Level Summary (P23 – Statistical Programming)

  • Acts as a leading expert and individual contributor.

  • Manages and supports projects/programs spanning multiple related areas.

  • Possesses comprehensive professional knowledge with measurable impact on department results.

  • Recognized as a valuable resource by peers.

  • Focuses on process improvement, design, and delivery of statistical programming outputs.


Additional Information

  • This description is not exhaustive; other duties may be assigned.

  • Equivalent skills, education, or experience will also be considered.

  • No employment contract is implied.

  • Fully compliant with EU Equality Directive and ADA (reasonable accommodations available).


Application

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