INTERNSHIP DETAILS

12-Month University Student Placement – Statistical Programming

CompanyFortrea
LocationLeeds
Work ModeOn Site
PostedOctober 7, 2026
Internship Information
Core Responsibilities
The intern will develop and maintain SAS programs to create clinical trial datasets and analysis outputs like Tables, Figures, and Listings. They will collaborate with global teams across Biostatistics and Data Management to support regulatory and scientific decision-making.
Internship Type
full time
Company Size
11486
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators. Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas. Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes. Together, exceptional is possible. Learn more at Fortrea.com
About the Role

12-Month University Student Placement – Statistical Programming – Leeds (Office-Based) – Start Date July 2027

 

At Fortrea, we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internship – it’s a launchpad for your future.


As a Statistical Programming Intern, you’ll join a global team where curiosity, problem-solving, and analytical thinking are celebrated. You’ll gain hands-on experience supporting real clinical trials, work alongside experienced programmers and statisticians, and learn how data drives the delivery of life-changing medicines.

We don’t expect you to know it all. What matters most is your potential, your drive to learn, and your willingness to grow. With mentorship, training, and real project involvement, we’ll help you build the technical and professional skills to succeed in the world of clinical research.

Your journey to pioneering tomorrow’s breakthroughs starts here.

 

Global Internship Program – From Campus to Business

As a Fortrea intern, from your very first day, you will complement your education in STEM or data analytics by contributing to real-world projects that align with our mission: to deliver solutions that bring life-changing medicines to patients faster and with true impact.


Your Team

The Statistical Programming Department plays a key role in the clinical development process. Our teams develop, validate, and maintain the programming solutions used to analyze and report clinical trial data. From study start-up through regulatory submission, we deliver accurate and reliable outputs that support scientific and business decision-making.


Internship Overview

This internship offers a unique opportunity to develop your programming, analytical, and data interpretation skills within a global, fast-paced environment.


Technical Development
You will gain exposure to tools and SAS language: you will develop and maintain SAS programs to create SDTM and ADaM datasets together with Tables, Figures, and Listings (TFLs).


Cross-Functional Collaboration
Work with global teams, including Biostatistics, Data Management, and Project Management, and experience how different disciplines come together to deliver successful trials.


Real-World Impact
Every dataset, analysis output, and report produced by our Statistical Programming teams contributes to the development of safe and effective therapies. Your work will play an important role in ensuring that clinical data is accurate, reliable, and ready to support regulatory and scientific decision-making.

 

And you’ll have fun while learning all that!

 

Education and Qualifications

  • You must be in your second year of a Bachelor’s degree in a quantitative or technical field such as Statistics, Mathematics, Computer Science, Data Science, Life Sciences, or another relevant discipline.
  • Demonstrated interest in clinical research, statistical programming, or data-driven problem-solving.
  • Ability to collaborate effectively with diverse, cross-functional teams.
  • Strong organizational and time management skills with attention to detail.
  • Proficiency in Microsoft Office, particularly Excel.
  • Familiarity with SAS, R, or other statistical software is an advantage but not required.

 

Other Key Skills

  • Analytical mindset and a passion for working with data.
  • Strong communication skills (both written and verbal).
  • Curiosity, adaptability, and a proactive approach to learning.
  • Ability to manage multiple priorities and meet deadlines.

 

Learn more about our EEO & Accommodations request here.

Key Skills
Statistical ProgrammingSASData AnalysisClinical TrialsSDTMADaMTFLsData ManagementBiostatisticsMicrosoft OfficeExcelAnalytical ThinkingProblem-solvingTime ManagementCommunication
Categories
Data & AnalyticsScience & ResearchHealthcareTechnologySoftware