Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead and support clinical trials using advanced statistical methods.
- Company: Join Cytel, a leader in clinical development and innovation.
- Benefits: Flexible remote work, competitive salary, and continuous professional development.
- Why this job: Make a real impact on 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 career 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.
Position Overview: Our Senior Biostatisticians lead and support clinical trials in different phases of development. They may also support activities at indication or compound level, perform ad-hoc or exploratory analyses, support submission activities 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. 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 and potentially integrated summaries for submissions
- Utilizing your strong communication skills to present and explain the methodology and consequences of decisions
- Understanding and following ICH and Health Authority regulations which affect the reporting of clinical trial data. This includes good clinical practice and guidelines for electronic submissions
- Driving and supporting publication related activities and ad-hoc requests
- Contribute to the creation, maintenance, documentation, and validation of standards for programming tools, outputs, and macros
- Participate in the review 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. is a plus.
- 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. Experience with Integrated Summaries for submission, safety reporting, regulatory questions etc. is a plus.
- Good SAS programming skills for QCing critical outputs, Efficacy/Safety tables, and working closely with Programmers. Knowledge of R programming is highly desirable.
- 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 communication skills: able to explain methodology and consequences of decisions in lay terms.
Senior Biostatistician FSP in London employer: Cytel Inc
Contact Detail:
Cytel Inc Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Biostatistician FSP in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals 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 researching the company and its recent projects. Tailor your responses to highlight how your skills as a Senior Biostatistician align with their goals. Show them you're not just another candidate, but someone who genuinely wants to contribute to their mission.
✨Tip Number 3
Practice your communication skills! As a biostatistician, you'll need to explain complex statistical concepts clearly. Run through common interview questions with a friend or mentor, focusing on how to make your answers engaging and easy to understand.
✨Tip Number 4
Don't forget to apply through our website! We love seeing applications directly from candidates who are excited about joining us. Plus, it gives you a chance to showcase your enthusiasm for the role right from the start.
We think you need these skills to ace Senior Biostatistician FSP in London
Some tips for your application 🫡
Show Your Passion: When writing your application, let your enthusiasm for clinical development shine through. We want to see that you're not just qualified, but genuinely excited about the role and the impact you can make.
Tailor Your CV: Make sure your CV is tailored to highlight your experience in biostatistics and clinical trials. We love seeing specific examples of how you've contributed to studies, so don’t hold back on the details!
Be Clear and Concise: In your cover letter, be clear and concise about why you’re a great fit for the Senior Biostatistician role. We appreciate straightforward communication, so get to the point while showcasing your skills.
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’s super easy to do!
How to prepare for a job interview at Cytel Inc
✨Know Your Stats
Brush up on your advanced statistical methods and be ready to discuss how you've applied them in clinical studies. Be prepared to explain sample size calculations and the development of statistical analysis plans (SAPs) in a way that shows your deep understanding.
✨Show Your Passion for Clinical Development
Demonstrate your enthusiasm for clinical trials and patient treatment innovations. Share specific examples of how you've motivated teams or contributed to pushing clinical development forward, as this aligns with what the company values.
✨Communicate Clearly
Practice explaining complex statistical concepts in simple terms. The ability to communicate effectively with both technical and non-technical stakeholders is crucial, so think of examples where you've successfully done this in the past.
✨Familiarise Yourself with Regulations
Make sure you understand ICH guidelines and Health Authority regulations that impact clinical trial data reporting. Being able to discuss these regulations and how they relate to your work will show that you're not just technically skilled but also compliant and aware of industry standards.
