At a Glance
- Tasks: Lead clinical studies and provide statistical expertise for innovative patient treatments.
- Company: Join a dynamic pharmaceutical client dedicated to advancing healthcare solutions.
- Benefits: Remote work, continuous training, and opportunities for professional growth.
- Other info: Work in a supportive environment with a focus on innovation and teamwork.
- Why this job: Make a real impact in clinical development while collaborating with top professionals.
- Qualifications: PhD or master's in statistics, clinical trial experience, and strong programming skills.
The predicted salary is between 60000 - 80000 £ per year.
Who Are You? 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.
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 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 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: As a Principal Biostatistician, your responsibilities will include:
- 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: 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:
- 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 communications skills.
- Ability to organize multiple work assignments and establish priorities.
- Working SAS & R programming knowledge required.
- CDISC knowledge required. Experience in R is preferred.
Remote Locations: United Kingdom, Spain, Netherlands, South Africa, Ireland, Sweden, Poland, Belgium
Sr. / Principal Biostatistician FSP - HTA (Remote Europe) in Preston employer: Cytel
Cytel is an exceptional employer that prioritises the growth and success of its employees, offering a dynamic work culture where innovation thrives. As a Principal Biostatistician, you will enjoy the autonomy to lead impactful clinical studies while being supported by a collaborative team dedicated to advancing patient treatment. With opportunities for continuous training and development, Cytel empowers you to push the boundaries of clinical development in a remote setting across Europe.
StudySmarter Expert Advice🤫
We think this is how you could land Sr. / Principal Biostatistician FSP - HTA (Remote Europe) in Preston
✨Tip Number 1
Network like a pro! Reach out to your connections in the biostatistics field, attend virtual meetups, and engage with professionals on LinkedIn. You never know who might have the inside scoop on job openings or can refer you directly.
✨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 projects. Practising common interview questions can also help you feel more confident when it’s your turn to shine!
✨Tip Number 3
Showcase your passion for innovation! When discussing your experience, highlight instances where you’ve pushed boundaries or introduced new methodologies. This will resonate well with companies looking for forward-thinking candidates like you.
✨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 are proactive about their job search and eager to join our mission in clinical development.
We think you need these skills to ace Sr. / Principal Biostatistician FSP - HTA (Remote Europe) in Preston
Some tips for your application 🫡
Show Your Passion:Let your enthusiasm for 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 biostatistics.
Tailor Your CV:Make sure your CV highlights your relevant experience in statistical analysis and HTA activities. We love seeing candidates who can clearly demonstrate their expertise and how it aligns with our needs.
Craft a Compelling Cover Letter:Use your cover letter to tell us why you're the perfect fit for this role. Share specific examples of your work and how you've contributed to successful clinical trials in the past.
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 Cytel.
How to prepare for a job interview at Cytel
✨Know Your Stats
Brush up on your statistical methods and biostatistical analysis techniques. Be ready to discuss how you've applied these in previous roles, especially in relation to HTA activities. This will show your expertise and confidence in the field.
✨Show Your Passion
Let your enthusiasm for clinical development shine through. Share examples of how you've motivated teams or pushed projects forward. Companies love candidates who are not just skilled but also genuinely excited about their work.
✨Prepare for Collaboration Questions
Since this role involves working closely with cross-functional teams, think of specific instances where you've successfully collaborated. Be prepared to discuss how you communicate and build relationships with clients and team members.
✨Master the Tech
Make sure you're comfortable discussing SAS and R programming. If you have experience with CDISC, highlight that too. Being able to talk about your technical skills confidently can set you apart from other candidates.
