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Statistical Programmer Ii

4+ years
Not Disclosed
10 July 18, 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 | ICON plc | Bangalore/Chennai/Trivandrum

Job Summary
ICON plc is seeking a skilled Senior Statistical Programmer with strong SAS programming and ADaM dataset development experience to support global clinical research projects. This hybrid role based in Bangalore, Chennai, or Trivandrum offers the opportunity to work on statistical programming for safety and efficacy analyses using CDISC standards in a collaborative environment focused on improving global healthcare outcomes.


Key Responsibilities

  • Create and validate safety and efficacy analysis datasets following CDISC and client-specific standards

  • Generate high-quality tables, listings, and figures (TLFs) for clinical trials

  • Develop programming specifications, mock-ups, and study-specific or general macros

  • Ensure quality, accuracy, and timely delivery of programming outputs

  • Organize and plan workload based on project timelines and deliverables

  • Troubleshoot and resolve programming issues effectively

  • Communicate and collaborate proactively with biostatistics teams and global stakeholders


Required Skills & Qualifications

  • Minimum 4+ years’ experience in ADaM programming for safety and efficacy domains

  • Proficiency in Base SAS, SAS Macros, PROC SQL, SAS/Stat, and SAS/Graph

  • Hands-on experience creating and validating TLFs

  • Familiarity with CDISC standards (SDTM, ADaM)

  • Strong problem-solving, documentation, and communication skills

  • Ability to work both independently and within a collaborative team environment


Perks & Benefits

  • Continuous professional development and training

  • Inclusive, diverse, and accessible work culture

  • Equal opportunity workplace

  • Opportunity to work on global clinical trials

  • Hybrid working flexibility


Company Description

ICON plc is a global leader in clinical research and healthcare intelligence, offering outsourced development services to pharmaceutical, biotech, and medical device companies. From molecule to medicine, ICON helps accelerate the delivery of life-saving treatments by leveraging innovation, data science, and dedicated healthcare professionals worldwide.


Work Mode: Hybrid (Bangalore, Chennai, or Trivandrum)
Preferred Experience: 4+ years in statistical programming within clinical research
Job Type: Full-time


Call to Action

Ready to make an impact in global clinical trials? Apply now to join ICON’s Biometrics team as a Senior Statistical Programmer and shape the future of clinical research.