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

Two computer monitors with data graphs
How Data Moves Through a Clinical Trial

Teaser label

Industry

Content type

Blogs

Publish date

12/01/2025

Summary

How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i

Teaser label

Discover how data flows through a clinical trial and learn where your skills could fit within clinical research.

Read more
Male and female auditing a manufacturing facility
Quality and Compliance - A Plain Language Guide

Teaser label

Industry

Content type

Blogs

Publish date

11/28/2025

Summary

Quality and Compliance for New Entrants:           A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job

Teaser label

A clear, practical introduction to quality and compliance for those starting a career in clinical research.

Read more
Female using a laptop to search for jobs
Improving Your Visibility in the Clinical Research Job Market

Teaser label

Career Progression

Content type

Blogs

Publish date

11/26/2025

Summary

How Clinical Research Job Seekers Can Enhance Their Applications Finding the right role in clinical research has become increasingly competitive as organisations continue to expand their study por

Teaser label

Discover the search terms recruiters use most often and practical steps that can help candidates strengthen their visibility.

Read more
View all

Similar jobs at ICON

Medical Research Associate(Phlebotomist/Medical Assistant)

Salary

Location

US, San Antonio, TX, IDS

Location

San Antonio

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinic

Job Type

Temporary Employee

Description

We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As an MRA at ICON, you will support the design, execution, and management of clinical trials and research st

Reference

JR138297

Expiry date

01/01/0001

Stephanie Curran Read more Shortlist Save this role
Clinical Data Science Programmer

Salary

Location

Colombia, Bogota

Location

Bogota

Mexico City

Remote Working

Remote

Business Area

ICON Strategic Solutions

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

JR137209

Expiry date

01/01/0001

Tulio Sanquiz

Author

Tulio Sanquiz
Read more Shortlist Save this role
Senior Specialist, Publications Operations

Salary

Location

Canada, Burlington

Location

Canada

Montreal

Burlington

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

The Publications Operations Senior Specialist is responsible for providing operational and administrative support to Publication Managers within the Publication Operations Team in Global Medical Affai

Reference

JR140391

Expiry date

01/01/0001

Kala Murphy

Author

Kala Murphy
Kala Murphy

Author

Kala Murphy
Read more Shortlist Save this role
Sr. CRA - São Paulo (FSP - Sponsor Dedicated)

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

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. As a Clinical Research Associate at ICON Plc, you will play a critical role in overseeing and managing clin

Reference

JR140016

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
CRA I or II

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Remote

Business Area

ICON Strategic Solutions

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

JR139582

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
CRA Careers in Italy

Salary

Location

Italy, Milan

Location

Milan

Remote Working

Office Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

From early-stage development to post-approval studies and commercialization strategies, our comprehensive services enable our partners to navigate the complex regulatory landscape and accelerate their

Reference

JR140389

Expiry date

01/01/0001

Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above