JUMP TO CONTENT

Senior Biostatistician II

JR068273

About the role

This vacancy has now expired. Please click here to view live vacancies.

Senior Biostatistician II

Location: Remote or Office based in India, Bangalore or EU.

We are the global Real World Evidence Strategy and Analytics team dedicated working on observational and real world evidence based trials for a number of indications.

As the Senior Biostatistician II you will develop statistical analysis plans and perform statistical analysis on assigned projects in accordance with study specifications, applicable guidelines, regulatory requirements and SOPs.

You will be expected to recognize the importance of and build a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting clients' needs.

About the role:

  • Supports study start-up activities (e.g. reviews, comments on and contributes to study design, protocols, case report forms).

  • Writes statistical methods sections of study protocols including sample size and power calculations with oversight.

  • Supports development of statistical analysis plans and develops table shells.

  • Reviews database specifications and leads initial review of raw variables and develops written specifications for derived variables from oral descriptions.

  • Programs basic statistical procedures and specialized statistical procedures (e.g., repeated measures, survival analysis, etc.) and/or SAS/Graph.

  • Develops complex macros for use by the group.

  • Develops deliverables, such as project reports and outputs, graphs, and tables with oversight.

  • Writes methods and results sections of final reports and publications such as abstracts, presentations, and manuscripts, with oversight.

  • Communicates with the client or investigator as needed.

  • May participate in professional activities including presentations at technical conferences (e.g. SAS meetings, ISPOR) with oversight.

Role Requirements

  • Demonstrable relevant experience at this level post Doctorate or Master's degree.

  • 5 years or more previous experience as a Statistician or SAS Programmer.

  • Proficient in SAS Data step with simple and complex conditional statements and variable creation, merges and concatenation

  • Experience using macros and arrays for repetitive tasks

  • Experience using descriptive statistics procedures for summarizing, restructuring, and outputting data

  • Experience using SAS Output Delivery System to control output from statistical procedures

  • Proficient in performing analyses using basic through advanced statistical procedures

Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below

List #1

Day in the life

Izabella's Journey Back to ICON

Teaser label

Our People

Content type

Blogs

Publish date

01/26/2026

Summary

Sometimes the best way to recognise what you have is to experience life without it. For Izabella Grimaldi, a Clinical Research Associate II based in Brazil, that realisation came after seven months wo

Teaser label

Izabella shares what makes our culture, leadership, and opportunities worth coming back for.

Read more
Asian female looking through microscope in lab
Understanding CRA, CTA, and SMA Roles in Clinical Research

Teaser label

Industry

Content type

Blogs

Publish date

01/20/2026

Summary

Understanding the Difference Between CRA, CTA, and SMA Clinical research job titles can be confusing, particularly for those new to the industry. Acronyms such as CRA, CTA and SMA appear frequentl

Teaser label

This guide explains the differences, responsibilities, and how each role supports clinical trial delivery.

Read more
video job interview
Interviewing at ICON

Teaser label

Inside ICON

Content type

Blogs

Publish date

01/05/2026

Summary

Interviewing at ICON: What to Expect Applying for a new role can feel uncertain, particularly when recruitment processes use digital tools or assessments that may be unfamiliar. At ICON, we want ca

Teaser label

Learn what to expect when interviewing at ICON, and how hiring decisions are always made by people.

Read more
View all

Similar jobs at ICON

Global Study Manager

Salary

Location

China, Shanghai

Department

Full Service - Corporate Support

Location

Shanghai

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successfu

Reference

JR143564

Expiry date

01/01/0001

Sunshine Yang

Author

Sunshine Yang
Read more Shortlist Save this role
Clinical Research Associate

Salary

Location

Japan, Tokyo

Department

Clinical Monitoring

Location

Tokyo

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordina

Reference

JR131783

Expiry date

01/01/0001

Emma Qu

Author

Emma Qu
Emma Qu

Author

Emma Qu
Read more Shortlist Save this role
Clinical Data Science Associate

Salary

Location

China, Dalian (PRA)

Location

Shanghai

Dalian

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Data Management

Job Type

Permanent

Description

We are currently seeking a Clinical Data Science Associate to join our diverse and dynamic team. As a Clinical Data Science Associate at ICON, you will play a key role in analyzing and interpreting cl

Reference

JR138502

Expiry date

01/01/0001

Xiangilan Liu

Author

Xiangilan Liu
Read more Shortlist Save this role
Senior Clinical Data Risk Analyst

Salary

Location

China, Beijing

Location

Beijing

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Data Operations Management

Job Type

Permanent

Description

We are currently seeking a Senior Clinical Data Risk Analyst to join our diverse and dynamic team. As a Senior Clinical Data Risk Analyst at ICON, you will play a pivotal role in identifying, assessin

Reference

JR141216

Expiry date

01/01/0001

Xiangilan Liu

Author

Xiangilan Liu
Read more Shortlist Save this role
Senior Clinical Research Associate

Salary

Location

Korea, Seoul

Location

Seoul

Remote Working

Office or Home

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical

Reference

JR143434

Expiry date

01/01/0001

Sonia Oh

Author

Sonia Oh
Sonia Oh

Author

Sonia Oh
Read more Shortlist Save this role
SSU lead Specialist

Salary

Location

China, Beijing

Location

Beijing

Shanghai

Remote Working

Office or Home

Business Area

ICON Strategic Solutions

Job Categories

Study Start Up

Job Type

Permanent

Description

We are currently seeking a Senior Study Start Up Associate to join our diverse and dynamic team. As a Senior Study Start Up Associate at ICON, you will be working within a large-scale, fast-paced envi

Reference

JR143304

Expiry date

01/01/0001

Allen Hao

Author

Allen Hao
Allen Hao

Author

Allen Hao
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above