Statistical Analyst
Role Overview
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.
Key Skills for This Role
Full Job Posting
About the role
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.
What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
Requirements
- 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.
About ICON plc
ICON is a publicly traded Irish clinical research organization serving pharmaceutical, biotechnology, medical-device, and public-health organizations.
Visit company websiteJobs and hiring trendsApply for this job in 1 click
Skip the repetitive application forms
Install the Base Career Chrome Extension and autofill job applications across major job boards with your profile.
Trusted by over 500,000 job seekers on Base Career
More from this employer
More jobs at ICON plc
Patient and Site Engagement Operations Specialist
, USA
Manager, Clinical Operations
, USA
Local Trial Management Base
, USA
Manager Clinical Operations
, USA
Senior Clinical Research Associate
, CAN
Senior Clinical System Lead
, USA
Senior Clinical Research Associate
, USA
Vice President, General Partner - Western US
, USA