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- Tasks: Lead clinical studies and provide statistical expertise for innovative patient treatments.
- Company: Join a global pharmaceutical client dedicated to advancing healthcare.
- Benefits: Empowerment, autonomy, and continuous training for your professional growth.
- Why this job: Make a real impact in clinical development with cutting-edge statistical methods.
- Qualifications: PhD or Master's in statistics, clinical trial experience, and SAS/R programming skills.
- Other info: Collaborative environment with opportunities for career advancement.
The predicted salary is between 36000 - 60000 £ per year.
An experienced Principal Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will lead one Phase I-IV clinical studies across your region. You are excited and enthusiastic, 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'll 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.
Our Principal Biostatisticians provide statistical and development support and influence for the associated client's trials providing expertise into processes, clinical development plans, concept sheets and protocols, as well as potentially providing oversight of work supported by other vendors. You will formulate integrated analytical approach to mine data sources, employ statistical methods, machine learning & deep learning algorithms to discover actionable insights and automate process for reducing effort and time for repeated use.
Responsibilities:
- Provide statistical input into planning and analysis of Indirect Treatment Comparison (ITC).
- Support Health Technology Assessment (HTA) dossier submission and negotiation.
- Create specifications and perform analyses such as time-to-event and longitudinal analysis.
- When in the Lead Biostatistician role for a project: manage biostatisticians and statistical programmers with respect to statistical strategy, deliverables and processes.
- Generate the use of innovative statistical methodology approaches by identifying, adapting, developing or using optimal statistical research methodologies and techniques appropriate to each project, and contribute internally and externally to the development and visibility of the company and of the Clinical Services department through her/his expertise and customer orientation.
- Develop strong collaboration and communication with sponsor cross-functional teams and sponsor Biostatistics management.
Qualifications:
- PhD in statistics or Master's degree in statistics or related subject required along with clinical trial experience.
- Relevant experience in statistical or biostatistical analysis supporting HTA activities.
- Understanding of the HTA-related guidelines.
- Excellent verbal and written communication skills.
- Ability to organize multiple work assignments and establish priorities.
- Working SAS & R programming knowledge required.
- CDISC knowledge required.
- Experience in R is preferred.
Principal Biostatistician FSP - HTA employer: Cytel (EMEA)
Contact Detail:
Cytel (EMEA) Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Biostatistician FSP - HTA
✨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. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on your statistical methods and clinical trial knowledge. We recommend practising common interview questions and even doing mock interviews with friends or mentors. The more confident you are, the better you'll perform!
✨Tip Number 3
Showcase your passion for innovation in biostatistics during interviews. Share examples of how you've pushed boundaries in previous roles or projects. We want to see that enthusiasm and drive to make a difference in clinical development!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us. Let’s get you on board!
We think you need these skills to ace Principal Biostatistician FSP - HTA
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 HTA activities. We love seeing how your background aligns with our needs, so don’t be shy about showcasing relevant projects and skills!
Craft a Compelling Cover Letter: Your cover letter is your chance to tell us why you’re the perfect fit for this role. Use it to explain how your expertise in statistical methods and clinical trials can contribute to our mission at Cytel.
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 Cytel (EMEA)
✨Know Your Stats
Brush up on your statistical methods and biostatistics principles. Be ready to discuss how you've applied advanced statistical techniques in previous projects, especially in relation to clinical trials and HTA activities.
✨Showcase Your Leadership Skills
As a Principal Biostatistician, you'll be leading teams. Prepare examples of how you've motivated and managed teams in the past. Highlight your ability to collaborate with cross-functional teams and how you’ve influenced project outcomes.
✨Understand the Client's Needs
Research the pharmaceutical client you'll be working with. Understand their current projects and challenges in clinical development. This will help you tailor your responses and show that you're genuinely interested in contributing to their success.
✨Prepare for Technical Questions
Expect questions about SAS, R programming, and CDISC standards. Be ready to discuss specific analyses you've performed, such as time-to-event or longitudinal analysis, and how you approached them. This will demonstrate your technical expertise and readiness for the role.
