Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Senior Statistical Programmer

Icon Plc
ICON PLC
7+ years
Not Disclosed
10 Jan. 22, 2026
Job Description
Job Type: Full Time Remote 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 Statistical Programmer – ICON India
Locations: Bangalore, Trivandrum, Chennai, India
Employment Type: Full-time
Work Mode: Office or Home (Flex)
Job ID: JR142358


About ICON

ICON plc is a global leader in healthcare intelligence and clinical research, dedicated to advancing innovative clinical solutions. We foster an inclusive and collaborative work environment, empowering professionals to grow while supporting the delivery of high-quality clinical trials worldwide.


Role Overview

ICON is seeking a Senior Statistical Programmer to join our dynamic team. This role is pivotal in analyzing clinical trial data, developing and validating statistical programs, and ensuring compliance with regulatory standards. You will collaborate closely with biostatisticians and cross-functional teams to contribute to the success of clinical studies and regulatory submissions.


Key Responsibilities

  • Develop, validate, and maintain SAS and R programs for statistical analysis and reporting of clinical trial data.

  • Collaborate with biostatisticians to define analysis plans and statistical methodologies.

  • Perform quality control checks to ensure accuracy, consistency, and reliability of statistical outputs.

  • Assist in the preparation of statistical reports, presentations, and publications for regulatory submissions.

  • Contribute to process improvements, optimizing programming practices and methodologies.


Candidate Profile

  • Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, or a related field.

  • 7+ years of experience in statistical programming, preferably in clinical research or pharmaceutical environments.

  • Strong proficiency in SAS and R programming, with a solid understanding of statistical concepts and methodologies.

  • Excellent analytical, problem-solving, and attention-to-detail skills.

  • Strong communication and collaboration skills, with the ability to effectively work in cross-functional teams and convey complex information.


Why Join ICON

  • Global Impact: Contribute to meaningful clinical trials and innovative treatments.

  • Career Growth: Access to training, mentorship, and opportunities to expand expertise.

  • Comprehensive Benefits: Health insurance, retirement planning, flexible work options, life assurance, wellness programs.

  • Inclusive Culture: ICON fosters diversity, equity, and belonging, creating a supportive workplace environment.