Senior Biostatistician II
Talent Acquisition Specialist
- Full Service Division
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
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
11/14/2025
Summary
Karina Espinoza's Journey at ICON Karina Espinoza's career in pharmacovigilance didn't begin with a grand plan. It started with a practical problem during her final year of a PhD in epidemiology, a
Teaser label
Our PeopleContent type
BlogsPublish date
11/13/2025
Summary
A Career Built on Patient Impact: Victoria DeVeaugh Geiss's Journey at ICON Victoria DeVeaugh Geiss has spent more than two decades in clinical research, and one thing has stayed constant throughout
Teaser label
IndustryContent type
BlogsPublish date
10/28/2025
Summary
Precision at the Outset: The Strategic Role of Site Selection and Activation in Clinical Trials The success of any clinical trial begins well before the first patient is enrolled. Behind every sit
Similar jobs at ICON
Salary
Location
Brazil, Sao Paulo
Location
Sao Paulo
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Regulatory Affairs
Job Type
Permanent
Description
We are currently seeking a Regulatory Scientist to join our diverse and dynamic team. As a Regulatory Scientist at ICON, you will complete country and/or regional Clinical Trial Regulatory deliverable
Reference
JR137458
Expiry date
01/01/0001
Author
Florencia Borello TaianaAuthor
Florencia Borello TaianaSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Trial Assistant (CTA) to join our diverse and dynamic team. As a Senior CTA at ICON Plc, you will play a key role in supporting the management and execution
Reference
JR138768
Expiry date
01/01/0001
Author
Ana TelloAuthor
Ana TelloSalary
Location
Israel, Tel Aviv
Location
Tel Aviv
Remote Working
Remote
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
JR138224
Expiry date
01/01/0001
Author
Salome KankiaAuthor
Salome KankiaSalary
Location
UK, Reading
Location
Reading
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Data Management
Job Type
Permanent
Description
We are currently seeking a Clinical Data Analyst to join our diverse and dynamic team. As a Clinical Data Analyst at ICON, you will play a key role in analyzing clinical trial data to support decision
Reference
JR138489
Expiry date
01/01/0001
Author
Elisabeth TrivicAuthor
Elisabeth TrivicSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and a
Reference
JR138765
Expiry date
01/01/0001
Author
Ana TelloAuthor
Ana TelloSalary
Location
France, Paris
Location
Paris
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Accounting & Finance
Job Type
Permanent
Description
We are now hiring an Investigator Payment Associate (Controleur de Gestion) and looking for highly dynamic and professionally sound aspirants like you to join our diverse and dynamic sponsor dedicate
Reference
JR139109
Expiry date
01/01/0001
Author
Dominique CarilienAuthor
Dominique Carilien