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

5+ years
Not Disclosed
10 Sept. 17, 2025
Job Description
Job Type: 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 Statistical Programmer (SAS / R, SQL)

Location:

Pune, India (Hybrid)

Job ID:

25101677

Company Overview:

Syneos Health® is a fully integrated biopharmaceutical solutions organization that accelerates customer success by combining clinical, medical affairs, and commercial expertise. Our Clinical Development model centers on patients and customers, streamlining processes to deliver therapies efficiently.

Learn more: Syneos Health


Job Summary:

The Senior / Principal Statistical Programmer (P23 level) develops statistical programs and provides programming support for statisticians and clients. This role involves creating analysis datasets, tables, listings, and graphs from complex clinical trial data. The professional acts as a subject matter expert, contributes to process improvement, and manages or directs lower-level staff in statistical programming activities.


Key Responsibilities:

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

  • Source, organize, and interpret complex clinical data sets to generate tables, listings, and graphs (TLGs).

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

  • Evaluate programming processes and suggest improvements to increase productivity.

  • Manage or contribute to projects, programs, or processes spanning multiple areas.

  • Direct or mentor lower-level professionals in statistical programming tasks.

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


Qualifications & Experience:

  • Minimum 5+ years of advanced SAS/R programming and SQL experience.

  • Hands-on experience in R programming, R package development, and SQL.

  • Experience with Python is a plus.

  • Knowledge of clinical domain, drug development process (Phase I-IV), and Clinical Data Management.

  • Study lead experience, capable of managing multiple studies.


Skills & Competencies:

  • Strong analytical, coding, and problem-solving skills.

  • Understanding of data visualization tools (TIBCO Spotfire or equivalent) and creation of calculated columns, markings, filtering, and document properties is preferred.

  • Excellent written and verbal communication skills.

  • Ability to manage multiple priorities and complex projects.


Impact and Contribution:

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

  • Provides expert-level support to statisticians and business teams.

  • Ensures data integrity and high-quality deliverables for clinical trial analysis.

  • Acts as a key resource and mentor within the statistical programming team.


Job Category:

  • Statistical Programming / Biostatistics / Clinical Data Management