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Statistical Analyst

India, Bangalore

Pay
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Work setting
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Employment
Full-time — employment source
Employment type in the employer’s listing: Full time
From the employer’s posting
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What you’ll work on

Full posting
  • Support study start-up with input on study design, protocols and case report forms

  • Assist in writing statistical analysis plans and creating table shells

  • Write derived variable specifications from oral descriptions

  • Program basic and specialized statistical procedures in SAS/Graph

  • Develop reports, graphs and tables under close oversight

From the employer’s posting
Support study start-up activities, providing valuable input on study design, protocols, and case report forms.
Assist in the development of statistical analysis plans and create table shells.
Develop written specifications for derived variables from oral descriptions.
Program basic and specialized statistical procedures, such as repeated measures and survival analysis, using SAS/Graph.
Develop deliverables, including project reports, graphs, and tables, with close oversight.

Tools in this posting

  • R
  • SAS
Source — Tool mentions in context
- 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.
- Review database specifications and lead the initial review of raw variables. Develop written specifications for derived variables from oral descriptions. - Program basic and specialized statistical procedures, such as repeated measures and survival analysis, using SAS/Graph. - Create complex macros for efficient group use.
- 4+ 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.

Posting record

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Status in our records
Live
First seen by us
Oct 7, 2026 · 18 days ago
Recorded sightings
69
Last seen by us
Oct 25, 2026

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Job description

View original posting ↗

Statistical Analyst- Office-Based (Bengaluru) / Home-Based

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 Analyst at ICON Plc, you will support clinical trial activities and collaborate with cross-functional teams to ensure the delivery of high-quality statistical analyses.

What You Will Do:

  • Support study start-up activities, providing valuable input on study design, protocols, and case report forms.
  • Write statistical methods sections of study protocols, including sample size and power calculations, with oversight.
  • Assist in the development of statistical analysis plans and create table shells.
  • Review database specifications and lead the initial review of raw variables. Develop written specifications for derived variables from oral descriptions.
  • Program basic and specialized statistical procedures, such as repeated measures and survival analysis, using SAS/Graph.
  • Create complex macros for efficient group use.
  • Develop deliverables, including project reports, graphs, and tables, with close oversight.

Your Profile:

  • 4+ 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

Source details

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Pay

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Location & working pattern

India, Bangalore

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Work authorization
- 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

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