Feasibility Data Scientist
Talent Acquisition Business Partner
- Full Service Division
About the role
This vacancy has now expired. Please click here to view live vacancies.
ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.
With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
The Feasibility Data Scientist is responsible for research and analysis of data to support proposal strategy, as well as site identification and selection decisions. The role also plays a vital part in researching, evaluating and implementing state-of-the-art informatics technologies to improve deliverables. Some specific duties include the following:
- Understand, guide and challenge the business in order to define analytics/dashboard requirements to drive department strategy
Model and transform complex datasets to enable optimal and scalable visualization and analytical options.
Develop the right visualisations in a variety of platforms (Spotfire, Power BI, Tableau etc) to enable clear and concise messaging to business users at different levels in the organization.
Create custom visualization types to complement out of the box standards
Effective management of concurrent projects to ensure rapid development and deployment.
Support proposal development, feasibility and site identification projects through the application of data and analytics expertise.
Use analytical tools to assess known and unknown information, uncertainties, and assumptions to provide probabilistic estimation of risks to study and program execution.
Communicate value of informatics tools to users and train them in the use of such tools.
Query relevant databases, including clinical trial registry tools and internal sources, and research various literature sources to support preparation of robust feasibility, site identification and selection deliverables.
Use analytical expertise to prepare risk benefit analyses and decision making criteria, while identifying opportunities to reduce cost without compromising quality.
Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, 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
IndustryContent type
BlogsPublish 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
IndustryContent type
BlogsPublish 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
Career ProgressionContent type
BlogsPublish 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
Similar jobs at ICON
Salary
Location
US, Blue Bell (ICON)
Location
Blue Bell
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Accounting & Finance
Job Type
Permanent
Description
We are currently seeking an Clinical Budget Analyst (Vendor) to join our diverse and dynamic team. As a Vendor CBA at ICON, you will play a pivotal role in determining fair market value pricing for in
Reference
JR140441
Expiry date
01/01/0001
Author
Brandon PupekAuthor
Brandon PupekSalary
Location
Australia, Melbourne
Department
Clinical Monitoring
Real World Solutions
Location
Melbourne
Sydney
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Contractor
Description
Role: Freelance Senior CRALocation: Sydney or MelbourneWe 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 p
Reference
JR139246
Expiry date
01/01/0001
Author
Krisztina AuthAuthor
Krisztina AuthSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Data Management
Job Type
Permanent
Description
We are currently seeking a Clinical Data Risk Analyst to join our diverse and dynamic team. As a Clinical Data Risk Analyst at ICON, you will play a crucial role in identifying and mitigating risks as
Reference
JR136188
Expiry date
01/01/0001
Author
Florencia Borello TaianaAuthor
Florencia Borello TaianaSalary
Location
Brazil, Sao Paulo
Location
Sao Paulo
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
Role : Clinical Trial ManagerLocation : Sao Paulo, BrazilWe are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsi
Reference
JR140560
Expiry date
01/01/0001
Author
Elizabeth DaviesAuthor
Elizabeth DaviesSalary
Location
Mexico, Mexico City
Department
Full Service - Clinical Operations
Location
Mexico City
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Regulatory Document Management
Job Type
Permanent
Description
Role : Trial Master File LeadLocation: Mexico (Homebased)We are currently seeking a Trial Master File Lead to join our diverse and dynamic team. As a TMF Lead at ICON, you will be responsible for over
Reference
JR138837
Expiry date
01/01/0001
Author
Elizabeth DaviesAuthor
Elizabeth DaviesSalary
Location
Greece, Athens
Department
Clinical Monitoring
Location
Athens
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Operations Management
Job Type
Permanent
Description
We are currently seeking a Manager, Clinical Operations to join our diverse and dynamic team. As a Manager, Clinical Operations at ICON, you will play a pivotal role in overseeing the execution of cli
Reference
JR140302
Expiry date
01/01/0001
Author
Lourdes Roy PratsAuthor
Lourdes Roy Prats