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- Tasks: Lead and support clinical studies using advanced statistical methods.
- Company: Join Cytel, a leader in clinical development and innovation.
- Benefits: Enjoy remote work flexibility, competitive salary, and continuous professional development.
- Why this job: Make a real impact in patient treatment and drive clinical development forward.
- Qualifications: Master's degree in statistics and 5+ years in clinical trials required.
- Other info: Collaborative environment with opportunities for growth and autonomy.
The predicted salary is between 36000 - 60000 £ per year.
An experienced Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will support or lead one or more Phase I-IV clinical studies. You are excited and enthusiastic. You motivate your teams to do great work and collaborate easily with your clients. You never settle for what is, but always push clinical development forward to what it could be.
Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Biostatistician you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.
Our Senior Biostatisticians perform ad-hoc or exploratory analyses to support submission or Health Authority Questions. Having exposure to regulatory work experience is a bonus, for example, if you understand the regulatory questions and translate them to statistical problems, collaborating effectively with clinical and regulatory colleagues. Supporting medium complexity clinical trials (starting from Design to Archival experience) and supporting some project-level activities.
Responsibilities
- Providing statistical support to clinical studies
- Participating in the development of study protocols, including participation in study design discussions and sample size calculations
- Reviewing CRFs and data review guidelines; developing statistical analysis plans (SAPs), including analysis dataset and TLG specifications
- Performing statistical analyses and interpreting statistical results
- Preparing clinical study reports, including integrated summaries for submissions
- Utilizing your strong communication skills to present and explain the methodology and consequences of decisions
- Understand and follow FDA regulations which affect the reporting of clinical trial data. This includes good clinical practice and guidelines for electronic submissions
- Contribute to the creation, maintenance, documentation, and validation of standards for programming tools, outputs, and macros
- Participate in the development of CRFs, edit check specifications, and data validation plans
- Provide review and/or author data transfer specifications for external vendor data
- Collaborate with internal and external functions (e.g. CROs, software vendors, clinical development partners, etc.) to ensure meeting project timelines and goals
- Provide review and/or author SOPs and/or Work Instructions related to statistical programming practices
Qualifications
Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:
- Master's degree in statistics or a related discipline. Ph.D. strongly desired.
- 5+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry.
- Experience working for a CRO is strongly desired.
- Experience in sample size calculation, protocol concept development, protocol development, SAP, and preparing clinical study reports including integrated summaries for submissions.
- Good SAS programming skills for QCing critical outputs, Efficacy/Safety tables, and working closely with Programmers. Knowledge of R programming is a plus.
- Solid understanding & implementation of CDISC requirements for regulatory submissions.
- Adept in ADaM specifications generation and QC of datasets.
- The ability to build strong external & internal relationships and motivate a regional or global team.
- Effective communicator: able to explain methodology and consequences of decisions in lay terms.
Senior/Principal Biostatistician FSP United Kingdom and 2 (Remote) Posted on 12/16/2025 Be the [...] in London employer: Cytel Inc
Contact Detail:
Cytel Inc Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior/Principal Biostatistician FSP United Kingdom and 2 (Remote) Posted on 12/16/2025 Be the [...] in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the biostatistics field, attend industry events, and engage on platforms like LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your statistical methods and clinical trial knowledge. Be ready to discuss how you've applied these in past roles. Practice common interview questions and think about how you can showcase your passion for clinical development.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. Check out our website for openings at Cytel and tailor your approach to show why you’re a perfect fit for their innovative environment.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. Use this opportunity to reiterate your enthusiasm for the role and how you can contribute to their team.
We think you need these skills to ace Senior/Principal Biostatistician FSP United Kingdom and 2 (Remote) Posted on 12/16/2025 Be the [...] in London
Some tips for your application 🫡
Show Your Passion: When writing your application, let your enthusiasm for biostatistics and clinical development shine through. We want to see that you're not just qualified, but genuinely excited about the role and how you can contribute to pushing clinical development forward.
Tailor Your CV: Make sure your CV is tailored to highlight your relevant experience in clinical trials and statistical methods. We love seeing specific examples of your work, especially those that align with the responsibilities listed in the job description.
Be Clear and Concise: In your cover letter and any written responses, keep it clear and to the point. We appreciate well-structured applications that communicate your skills and experiences without unnecessary fluff. Remember, clarity is key!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about what we do at StudySmarter.
How to prepare for a job interview at Cytel Inc
✨Know Your Stats
Brush up on your statistical methods and clinical trial knowledge. Be ready to discuss how you've applied advanced statistical techniques in past projects, especially in Phase I-IV studies. This will show your expertise and passion for the role.
✨Showcase Your Communication Skills
Prepare to explain complex statistical concepts in simple terms. Think of examples where you successfully communicated methodologies or results to non-statistical colleagues. This is crucial for collaborating with clinical and regulatory teams.
✨Understand Regulatory Requirements
Familiarise yourself with FDA regulations and CDISC requirements. Be prepared to discuss how you've navigated these in previous roles, as this will demonstrate your ability to handle regulatory questions and submissions effectively.
✨Demonstrate Team Motivation
Think of instances where you've motivated your team or collaborated with clients. Share specific examples that highlight your leadership skills and ability to drive projects forward, as this aligns perfectly with what the company values.
