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Senior Statistical Programmer I

6+ years
Not Disclosed
10 June 26, 2025
Job Description
Job Type: Full Time 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

 

Senior Statistical Programmer – Hybrid (Bangalore/Chennai/Trivandrum)

Job Summary:

ICON plc is hiring a Senior Statistical Programmer to support global clinical trials across safety and efficacy domains. This hybrid role in Bangalore, Chennai, or Trivandrum involves programming ADaM datasets, creating validated TLFs, and working in compliance with CDISC standards. If you're an expert in SAS and CDISC with 6+ years of experience, this is your opportunity to drive impactful healthcare research.


Key Responsibilities:

  • Develop and validate ADaM datasets aligned with CDISC and sponsor standards.

  • Generate high-quality safety and efficacy Tables, Listings, and Figures (TLFs).

  • Create and maintain reusable programming macros and mock-ups.

  • Collaborate with biostatistics and clinical teams to meet study timelines.

  • Document all programming work to ensure audit readiness and compliance.

  • Troubleshoot programming issues and propose effective solutions.

  • Plan and monitor tasks to ensure delivery in accordance with KPIs and quality benchmarks.

  • Support cross-functional communication and collaboration across global teams.


Required Skills & Qualifications:

  • Minimum 6 years of experience in statistical programming for clinical trials.

  • Hands-on expertise in ADaM programming for safety and efficacy datasets.

  • Advanced proficiency in SAS/Base, SAS Macros, PROC SQL, SAS/Stat, SAS/Graph.

  • Solid understanding of CDISC standards, including SDTM and ADaM.

  • Familiarity with clinical data standards and regulatory guidelines (e.g., ICH-GCP).

  • Strong communication, problem-solving, and organizational skills.

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


Perks & Benefits:

  • Competitive base pay with variable pay and recognition programs.

  • Comprehensive employee benefits tailored to support personal and family needs.

  • Learning and development opportunities in a growth-focused environment.

  • Inclusive and discrimination-free workplace.

  • Long-term career support and wellbeing initiatives.


Company Description:

ICON plc is a global leader in healthcare intelligence and clinical research, offering outsourced development and commercialisation services to pharmaceutical, biotechnology, and medical device companies. With operations across the globe, ICON is driven by innovation, quality, and a mission to improve patient outcomes through accelerated drug and device development.


Work Mode:

Hybrid – Based in Bangalore, Chennai, or Trivandrum


Call-to-Action:

If you’re ready to take the next step in your clinical programming career, apply today and become a part of ICON’s mission to improve lives through research.