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- Tasks: Design and analyse clinical trials, impacting innovative therapies.
- Company: Fortrea is a leading CRO focused on pioneering clinical research.
- Benefits: Enjoy remote work flexibility, competitive salary, and career growth opportunities.
- Why this job: Make a real difference in patient lives while collaborating with diverse professionals.
- Qualifications: 5-10 years of biostatistics experience and advanced degree required.
- Other info: Join a supportive team dedicated to revolutionising clinical trial processes.
The predicted salary is between 48000 - 84000 ÂŁ per year.
Senior and Principal Biostatistician – FSP
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Senior and Principal Biostatistician – FSP
3 days ago Be among the first 25 applicants
Join to apply for the Senior and Principal Biostatistician – FSP role at Fortrea
Fortrea is looking for Senior and Principal Biostatisticians to join our sponsor dedicated team
As a Senior Biostatistician at Fortrea, you will play a crucial role in the design, analysis, and interpretation of clinical trials, directly impacting the development of innovative therapies and treatments. Supported by a diverse team of research professionals, you will collaborate closely with study teams, medical experts, and project managers to ensure the highest quality scientific research and statistical analysis.
Your Responsibilities
- Design and implement statistical strategies for clinical trials within various therapeutic areas.
- Develop statistical analysis plans, ensuring their appropriateness for study objectives.
- Perform statistical programming tasks using SAS for analyses and generate study reports.
- Collaborate with cross-functional study teams to contribute statistical expertise and guidance.
- Provide expertise on statistical methodology, sample size calculations, and innovative trial design.
- Ensure the quality and integrity of statistical deliverables.
- Oversight of all the statistical queries on multiple projects.
Your Experience And Qualifications
- Minimum of 5 years (Senior) or 10 years (Principal) of experience as a Biostatistician within a CRO, biotech or pharmaceutical company.
- Solid understanding of statistical methods commonly used in clinical trials, including advanced concepts.
- Extensive knowledge of CDISC standards.
- Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs
- Proven professional experience with SDTMs, ADaM datasets and TFLs
- Strong knowledge of regulatory guidelines (e.g., FDA, EMA) and industry standards.
- Excellent communication skills, with the ability to effectively collaborate and present complex data to non-technical audiences.
- Advanced degree (Ph.D. or Master’s) in Biostatistics, Statistics, or a related field.
- Demonstrated ability to work independently, utilize problem-solving skills, and make sound decisions.
What You Can Expect From Us
- Pioneering Research: Join a CRO at the forefront of clinical trials within multiple therapeutic areas.
- Career Growth: Expand your skill set and broaden your expertise in a supportive and environment, with numerous opportunities for career advancement.
- Impactful Work: Contribute directly to the development of groundbreaking therapies and treatments, improving the lives of patients worldwide.
- Competitive Compensation: We offer a competitive salary package, comprehensive benefits, and a rewarding bonus structure.
- Life-Style: Flexibility to work remotely from anywhere, promoting a healthy work-life balance.
You can be 100% home-based in any of the EMEA locations listed on this ad
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea Is Proud To Be An Equal Opportunity Employer
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
If, As a Result Of a Disability, You Require a Reasonable Accommodation To Complete Your Job Application, Pre-employment Testing, Job Interview Or To Otherwise Participate In The Hiring Process, Please Contact
taaccommodationsrequest@fortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.
Learn more about our EEO & Accommodations request here.
Seniority level
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Seniority level
Mid-Senior level
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Employment type
Full-time
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Job function
Research, Analyst, and Information Technology
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Senior and Principal Biostatistician - FSP employer: Fortrea
Contact Detail:
Fortrea Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior and Principal Biostatistician - FSP
✨Tip Number 1
Network with professionals in the biostatistics field, especially those who work at Fortrea or similar companies. Attend industry conferences or webinars to connect with potential colleagues and learn more about the company culture.
✨Tip Number 2
Familiarise yourself with the latest advancements in statistical methodologies and clinical trial designs. Being able to discuss recent trends or innovations during an interview can set you apart from other candidates.
✨Tip Number 3
Prepare to demonstrate your proficiency in SAS programming. Consider working on sample projects or case studies that showcase your ability to debug SAS programs and generate reports, as this is a key requirement for the role.
✨Tip Number 4
Research Fortrea's recent projects and therapeutic areas they focus on. Being knowledgeable about their work will not only help you tailor your responses but also show your genuine interest in contributing to their mission.
We think you need these skills to ace Senior and Principal Biostatistician - FSP
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in biostatistics, particularly within clinical trials. Emphasise your knowledge of statistical methods, SAS programming, and any experience with CDISC standards.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for biostatistics and your understanding of the role at Fortrea. Mention specific projects or experiences that demonstrate your ability to design and implement statistical strategies.
Highlight Communication Skills: Since the role requires excellent communication skills, provide examples in your application of how you've effectively collaborated with cross-functional teams or presented complex data to non-technical audiences.
Showcase Problem-Solving Abilities: In your application, include instances where you've successfully solved problems or made sound decisions in your previous roles. This will demonstrate your capability to work independently and contribute to innovative trial designs.
How to prepare for a job interview at Fortrea
✨Showcase Your Statistical Expertise
Be prepared to discuss your experience with statistical methods and how you've applied them in clinical trials. Highlight specific projects where you designed statistical analysis plans or implemented innovative trial designs.
✨Demonstrate SAS Proficiency
Since SAS programming is crucial for this role, be ready to talk about your experience with base SAS, SAS macros, and debugging SAS programs. You might even want to prepare a few examples of how you've used SAS to generate study reports.
✨Understand Regulatory Guidelines
Familiarise yourself with regulatory guidelines such as those from the FDA and EMA. Be prepared to discuss how these guidelines influence your work and ensure the quality and integrity of statistical deliverables.
✨Communicate Complex Data Effectively
Since you'll need to present complex data to non-technical audiences, practice explaining your statistical findings in simple terms. This will demonstrate your communication skills and ability to collaborate with cross-functional teams.
