Instagram
youtube
Facebook

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:

Gurugram, India (Hybrid)

Job ID:

25101677

Company Overview:

Syneos Health® is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success. By combining clinical, medical affairs, and commercial insights, the company streamlines processes to deliver therapies efficiently.

Learn more: Syneos Health


Job Summary:

The Senior / Principal Statistical Programmer (P23 level) develops statistical programs and provides advanced programming support for statisticians, clients, and business use. The role involves sourcing, organizing, and interpreting complex clinical trial data to produce analysis datasets, tables, listings, and graphs (TLGs). As a subject matter expert, the professional evaluates programming processes, mentors lower-level staff, and contributes to process improvements.


Key Responsibilities:

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

  • Source, organize, and interpret complex data sets to generate tables, listings, and graphs.

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

  • Evaluate programming processes and propose revisions to improve productivity.

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

  • Direct or mentor lower-level statistical programmers.

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


Qualifications & Experience:

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

  • Experience in R programming, R package development, and SQL.

  • Hands-on Python knowledge is a plus.

  • Understanding 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.

  • Knowledge of data visualization tools (TIBCO Spotfire or equivalent) preferred.

  • Excellent written and verbal communication skills.

  • Ability to manage multiple priorities and complex projects effectively.


Impact and Contribution:

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

  • Ensures integrity, quality, and timely delivery of clinical trial data outputs.

  • Provides expert-level support and contributes to organizational, functional, and departmental targets.


Job Category:

  • Statistical Programming / Biostatistics / Clinical Data Management