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- Tasks: Develop and validate SAS programs for life-changing oncology clinical trials.
- Company: Join Fortrea, a leader in global oncology clinical trials.
- Benefits: 100% home-based role with competitive salary and professional growth.
- Why this job: Make a real impact on cancer therapies while working remotely.
- Qualifications: Degree in relevant field and 4+ years in oncology clinical trials required.
- Other info: Collaborative environment with opportunities for process improvement and innovation.
The predicted salary is between 36000 - 60000 ÂŁ per year.
Senior or Principal Statistical Programmer – Oncology
Join Fortrea as a Senior or Principal Statistical Programmer in our sponsor‑dedicated Flexible Solutions business unit, central to the delivery of complex global oncology clinical trials (Phases I–III) for world‑renowned pharmaceutical companies.
As a 100% home‑based role (or office in your home country), you will contribute to the development of life‑changing oncology therapies by developing and validating SAS programs for data analysis and reporting, supporting submissions, regulatory responses, publications, and post‑hoc requests.
Your Responsibilities
- Perform programming activities for oncology clinical trials, ensuring quality, accuracy, and compliance with study timelines and regulatory standards.
- Review SAPs and TFL shells from a programming perspective, providing technical input to optimize oncology analyses.
- Advise on the design and development of complex TFL shells and statistical outputs for oncology studies.
- Develop and/or lead the creation of specifications for SDTM and ADaM datasets.
- Develop and maintain SAS programs to create SDTM and ADaM datasets and generate Tables, Figures, and Listings; perform thorough quality control checks.
- Produce and validate Define.xml/PDFs, Analysis Results Metadata (ARM), annotated CRFs, and Reviewers’ Guides to support SDTM and ADaM submissions.
- Contribute to the preparation of regulatory submission packages and responses to regulatory and client audits.
- Identify, propose, and implement process improvements to enhance programming efficiency, quality, and standardization.
- Stay up to date on industry standards, global regulatory requirements, Fortrea SOPs, and CDISC developments relevant to oncology data.
Your Profile
- Degree in a relevant field such as Mathematics, Life Sciences, Statistics, or Computer Science.
- Equivalent vocational training and/or significant professional experience in clinical statistical programming may be considered.
- Minimum of 4 years’ hands‑on experience in oncology clinical trials is required.
- Proven experience with SAS programming (Base SAS, SAS Macros, SAS/STAT) and ability to debug complex programs.
- Strong practical knowledge of CDISC standards (SDTM, ADaM) and experience generating safety and efficacy reporting outputs for Phase III oncology studies.
- Experience with regulatory submission deliverables, including Define.xml, ARM, and reviewers’ guides.
- Strong organizational skills with an autonomous yet collaborative working style.
- A curious and analytical mindset, with a keen eye for detail and quality.
- Business fluency in English, both spoken and written.
Learn more about our EEO & Accommodations request here.
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Senior or Principal Statistical Programmer - ONCOLOGY - Sponsor dedicated employer: Fortrea
Contact Detail:
Fortrea Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior or Principal Statistical Programmer - ONCOLOGY - Sponsor dedicated
✨Tip Number 1
Network like a pro! Reach out to professionals in the oncology field on LinkedIn or at industry events. A friendly chat can lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Show off your skills! Prepare a portfolio of your SAS programming projects and any relevant work you've done in oncology trials. This will give you an edge during interviews and showcase your expertise.
✨Tip Number 3
Practice makes perfect! Get ready for technical interviews by brushing up on your SAS programming skills and understanding CDISC standards. Mock interviews with friends can help you feel more confident.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Senior or Principal Statistical Programmer - ONCOLOGY - Sponsor dedicated
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the role of Senior or Principal Statistical Programmer. Highlight your experience in oncology clinical trials and your SAS programming skills, as these are key for us at Fortrea.
Craft a Compelling Cover Letter: Your cover letter should tell us why you're passionate about oncology and how your background makes you a great fit. Don’t just repeat your CV; use this space to showcase your personality and enthusiasm for the role.
Showcase Relevant Experience: When detailing your experience, focus on specific projects or achievements that relate to the responsibilities listed in the job description. We want to see how you've contributed to successful oncology trials in the past.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at Fortrea
✨Know Your SAS Inside Out
Make sure you brush up on your SAS programming skills before the interview. Be prepared to discuss specific projects where you've used Base SAS, SAS Macros, and SAS/STAT. They’ll likely want to hear about how you debugged complex programs, so have some examples ready!
✨Understand CDISC Standards
Familiarise yourself with CDISC standards, especially SDTM and ADaM. You might be asked to explain how you've applied these standards in previous roles, so think of concrete examples where you developed or validated datasets for oncology studies.
✨Showcase Your Problem-Solving Skills
Be ready to discuss how you've identified and implemented process improvements in your past work. Think of specific instances where your analytical mindset led to enhanced programming efficiency or quality, as this will demonstrate your proactive approach.
✨Prepare for Regulatory Discussions
Since regulatory submissions are a key part of the role, review your experience with deliverables like Define.xml and Analysis Results Metadata. Be prepared to talk about how you contributed to submission packages and any challenges you faced during audits.
