ICON

Statistical Programmer II

India · Work style not stated · Full time

Apply on the employer’s site ↗See how well you match this job

You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.

About the role

Description from the employer’s posting. Check the employer’s page for the current version.

EmployerICON
LocationIndia
Work styleWork style not stated
Employment typeFull time
Employer posted6 Oct 2026

Statistical Programmer II

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Statistical Programmer II at ICON, you will the development, validation, and execution of statistical programs to support clinical trial analysis and reporting.

What You Will Do:

Developing, validating, and maintaining complex statistical programs (SAS, R, or similar) for data manipulation, analysis, and reporting in phase IV trials and peri/post approval studies
Collaborating with biostatisticians and cross-functional teams to interpret study requirements and ensure the accurate implementation of statistical analyses.
Preparing and reviewing statistical analysis plans (SAPs), programming specifications, and derived datasets to meet regulatory standards.
Ensuring data integrity and compliance with industry regulations, including ICH/GCP guidelines, throughout the programming process.
Mentoring junior programmers and assisting in training team members on programming techniques and best practices.

Show full description

Your Profile:

2+ years of statistical programming experience within the pharmaceutical, biotechnology, or CRO industry.
Strong hands-on expertise in SAS programming, with experience supporting clinical trial deliverables and statistical analyses.
Basic knowledge, training, or exposure to R programming, with a willingness to expand proficiency in a clinical research environment.
Comprehensive understanding of CDISC standards, including SDTM and ADaM.
Experience developing, validating, and maintaining production-quality programming code.
Experience using Pinnacle 21 (P21) for CDISC compliance checks and data validation.
Excellent analytical, problem-solving, and communication skills, with the ability to collaborate effectively across cross-functional teams.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

See how well you match this job Apply on the employer’s site ↗

Check your resume against this job Free, no sign-up. Nothing you paste is stored.

Staying safe while you apply

Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.

Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.

Preparing for this role with ROLIVA

Check the fit.
Compare the requirements with the experience you have confirmed, including gaps.
Prepare honestly.
Build interview stories and application drafts from your own evidence.
Keep track.
Save the role and record your own application status and follow-ups.

Create a free workspace or log in.