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- Tasks: Support clinical studies with advanced statistical methods and collaborate with teams.
- Company: Join a leading pharmaceutical client driving innovative patient treatments.
- Benefits: Competitive salary, flexible work environment, and opportunities for professional growth.
- Why this job: Make a real impact in clinical development and empower patient care.
- Qualifications: Master's degree in statistics; 3+ years in clinical trials; SAS programming skills.
- Other info: Dynamic role with strong team collaboration and career advancement opportunities.
The predicted salary is between 36000 - 60000 £ per year.
A Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will support 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. You motivate others to do the same.
Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you will be at the heart of our client’s innovation. As a 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.
As a Biostatistician, you will 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 translating them to statistical problems, collaborating effectively with clinical and regulatory colleagues.
RESPONSIBILITIESAs a Biostatistician, your responsibilities will include:
- 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.
Master's degree in statistics or a related discipline. Ph.D. strongly desired.
- 3+ 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 in London employer: Cytel - EMEA
Contact Detail:
Cytel - EMEA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior / Principal Biostatistician FSP in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the biostatistics field, especially those who work in clinical development. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Show off your skills! Prepare a portfolio of your past projects and analyses. When you get the chance to meet potential employers, having tangible examples of your work can really set you apart from the crowd.
✨Tip Number 3
Practice makes perfect! Before any interviews, do some mock sessions with friends or mentors. Focus on explaining complex statistical concepts in simple terms, just like you would to a client or colleague.
✨Tip Number 4
Don’t forget to apply through our website! We’re always on the lookout for passionate Biostatisticians. Your next big opportunity could be just a click away, so make sure to check it out regularly!
We think you need these skills to ace Senior / Principal Biostatistician FSP in London
Some tips for your application 🫡
Show Your Passion: Let your enthusiasm for biostatistics and clinical development shine through in your application. We want to see how excited you are about the role and how you can motivate others to push boundaries in clinical research.
Tailor Your CV: Make sure your CV highlights relevant experience, especially in clinical trials and statistical analysis. We love seeing specific examples of your work that align with the responsibilities listed in the job description.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you're the perfect fit for this role. Share your journey in biostatistics, your understanding of regulatory processes, and how you can contribute to our client's innovation.
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 this exciting opportunity with our pharmaceutical client.
How to prepare for a job interview at Cytel - EMEA
✨Know Your Stats
Brush up on your statistical methods and be ready to discuss how you've applied them in clinical studies. Be prepared to explain complex concepts in simple terms, as effective communication is key for this role.
✨Showcase Your Experience
Highlight your experience with clinical trials, especially any work with CROs. Be specific about your contributions to study protocols, sample size calculations, and statistical analysis plans. Use examples that demonstrate your ability to motivate teams and collaborate effectively.
✨Understand the Regulatory Landscape
Familiarise yourself with regulatory requirements and how they relate to biostatistics. Be ready to discuss any past experiences where you translated regulatory questions into statistical problems, showcasing your problem-solving skills.
✨Prepare Questions
Think of insightful questions to ask about the company’s current projects and future directions. This shows your enthusiasm for the role and helps you gauge if the company aligns with your career goals. It’s a two-way street!
