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

Nurse and patient
Understanding Roles in a Clinical Trial: Sponsors, CROs, and Sites

Teaser label

Industry

Content type

Blogs

Publish date

02/16/2026

Summary

What Sponsors, CROs, and Sites Each Do Clinical research brings together many organisations, each with a specific role in delivering a clinical trial. For those new to the industry, the relationsh

Teaser label

Learn how clinical trials are delivered by understanding the roles of sponsors, CROs, and sites.

Read more
Key skills that make candidates successful in FSP roles

Teaser label

Industry

Content type

Blogs

Publish date

02/16/2026

Summary

Functional Service Provision (FSP), also known as sponsor-embedded delivery, is a core part of how modern clinical research is delivered. At ICON Strategic Solutions, our teams work as an extens

Teaser label

In this blog, we outline the key skills and attributes that help professionals thrive in FSP environments and build long term careers in sponsor-embedded roles.

Read more
Headshot of female
From Lab Bench to Program Leadership: Sinéad McKeon's Career at ICON

Teaser label

Our People

Content type

Blogs

Publish date

02/05/2026

Summary

Building expertise through diverse roles and continuous learning Sinéad McKeon's career at ICON demonstrates how scientific training can evolve into strategic leadership. Now a Senior Manager in Lab

Teaser label

Discover how a career can evolve from hands on lab work to program management in this interview with Sinéad McKeon.

Read more
View all

Similar jobs at ICON

Senior TMF Specialist

Salary

Location

India, Chennai

Department

Clinical Trial Management

Location

Chennai

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Regulatory Document Management

Job Type

Permanent

Description

We are currently seeking a Senior TMF Specialist to join our diverse and dynamic team. As a Senior TMF Specialist at ICON, you will play a pivotal role in managing the Trial Master File (TMF) for clin

Reference

JR146301

Expiry date

01/01/0001

Persis Davis

Author

Persis Davis
Read more Shortlist Save this role
CLINICAL TRIAL ASSOCIATE

Salary

Location

China, Shanghai

Location

Shanghai

Remote Working

Remote or Office

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

We are currently seeking a Clinical Trial Associate to join our diverse and dynamic team. As a Clinical Trial Associate at ICON, you will play a pivotal role in assisting with the design and analysis

Reference

JR146052

Expiry date

01/01/0001

Jenny Zhang

Author

Jenny Zhang
Jenny Zhang

Author

Jenny Zhang
Read more Shortlist Save this role
Clinical Research Associate II/ Senior CRA

Salary

Location

Czech Republic, Prague

Department

Clinical Monitoring

Location

Prague

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing cli

Reference

JR146285

Expiry date

01/01/0001

Tereza Svobodova Read more Shortlist Save this role
Clinical Data Science Programmer

Salary

Location

India, Bangalore

Location

Bangalore

Chennai

Trivandrum

Bengaluru

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Programming

Job Type

Permanent

Description

We are currently seeking a Clinical Data Science Programmer to join our diverse and dynamic team. As a Clinical Data Science Programmer at ICON, you will play an essential role in developing and imple

Reference

JR146195

Expiry date

01/01/0001

Kavitha K

Author

Kavitha K
Kavitha K

Author

Kavitha K
Read more Shortlist Save this role
Clinical Research Associate

Salary

Location

Korea, Seoul

Location

Seoul

Remote Working

Remote

Business Area

ICON Strategic Solutions

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

JR146256

Expiry date

01/01/0001

Sonia Oh

Author

Sonia Oh
Sonia Oh

Author

Sonia Oh
Read more Shortlist Save this role
Global Operations Quality Manager

Salary

Location

Canada, Burlington

Location

Montreal

Raleigh

Burlington

Blue Bell

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Quality Assurance

Job Type

Permanent

Description

Quality and GCP OversightProvide quality consultation within assigned scope, escalating complex or enterprise- impacting issues to the Senior Global Quality Manager and/or Global Head - GCP Excellence

Reference

JR145584

Expiry date

01/01/0001

Jamie Pruitt

Author

Jamie Pruitt
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above