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For Companies At a Glance
- Tasks: Lead statistical work for clinical trials, proposing innovative designs and methodologies.
- Company: Join Novartis, a leader in drug development committed to diversity and inclusion.
- Benefits: Enjoy a supportive environment with personal and professional growth opportunities.
- Why this job: Make a real impact in healthcare while collaborating with diverse teams.
- Qualifications: MS or PhD in Statistics with relevant experience; strong communication skills required.
- Other info: Work independently on complex trials and contribute to groundbreaking drug development.
The predicted salary is between 54000 - 84000 £ per year.
Overview
Office Location: London (The Westworks), United Kingdom
Hybrid (12 days per month on-site if living within 50 miles of our London office)
Remote (if living beyond 50 miles of our London office)
About The Role
We are in search of a Senior Principal Biostatistician to join a passionate team within Advanced Quantitative Sciences. Come to an industry leader where you will lead implementation of modern and innovative trial/experimental designs, statistical models, analysis and data exploration methodologies at the study level and you will be responsible for all statistical work, scientific and operational, in collaboration with the clinical trial teams and other quantitative partners
Your Key Responsibilities
- Responsible for all statistical tasks on the assigned trials.
- Protocol development in alignment with the development plan, developing statistical analysis plan, reporting activities.
- Contribute to planning and execution of exploratory analyses and statistical consultation within your cross-functional teams.
- Initiate, drive and implement novel methods and innovative trial designs in alignment with the Lead Statistician.
- Collaborate with clinical, regulatory and other strategic functions to drive quantitative decision making in assigned indications/program with oversight.
- Collaborate cross-functionally (e.g. data management, programming, medical writing) to ensure timeliness and quality of statistical deliverables.
- Contribute to external engagement with consultants, advisory boards, health authorities, congresses, and scientific meetings
Role Requirements
Essential Requirements
- PhD experience preferred OR MS with extensive experience
- Fluent English (oral and written)
- Strong communication and presentation skills
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
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Senior Principal Biostatistician employer: Novartis
Contact Detail:
Novartis Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Principal Biostatistician
✨Tip Number 1
Familiarise yourself with the latest statistical methodologies and innovative trial designs. Being able to discuss these concepts confidently during interviews will demonstrate your expertise and readiness for the role.
✨Tip Number 2
Network with professionals in the biostatistics field, especially those who have experience in clinical trials. Attend relevant conferences or webinars to make connections and learn about industry trends that could give you an edge.
✨Tip Number 3
Prepare to explain complex statistical concepts in simple terms. This skill is crucial for collaborating with non-statistical team members and will showcase your ability to communicate effectively across functions.
✨Tip Number 4
Stay updated on drug development processes and Health Authority guidelines. Understanding these regulations will not only help you in the role but also impress interviewers with your commitment to compliance and quality.
We think you need these skills to ace Senior Principal Biostatistician
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in biostatistics, particularly in clinical trials. Emphasise your proficiency with statistical software like SAS or R, and any specific methodologies you've implemented.
Craft a Strong Cover Letter: In your cover letter, clearly articulate your understanding of the role and how your skills align with the responsibilities outlined. Mention your experience with innovative trial designs and your ability to communicate complex statistical concepts to non-statisticians.
Showcase Relevant Projects: Include specific examples of past projects where you led statistical activities or contributed to drug development. Highlight your role in protocol development and any successful collaborations with cross-functional teams.
Proofread and Edit: Before submitting your application, thoroughly proofread your documents for clarity and grammatical accuracy. A well-presented application reflects your attention to detail, which is crucial in biostatistics.
How to prepare for a job interview at Novartis
✨Showcase Your Statistical Expertise
Be prepared to discuss your experience with statistical methodologies and how you've applied them in clinical trials. Highlight specific examples where you proposed innovative designs or models, as this role requires a strong foundation in statistics.
✨Communicate Clearly
Since you'll need to explain complex statistical concepts to non-statisticians, practice simplifying your explanations. Use relatable analogies or examples to demonstrate your ability to communicate effectively across different functions.
✨Demonstrate Leadership Skills
This position involves leading statistical activities with limited supervision. Be ready to share instances where you've taken the initiative in projects, driven change, or influenced decisions that impacted trial outcomes.
✨Familiarise Yourself with Regulatory Guidelines
Understanding drug development processes and Health Authority guidelines is crucial. Brush up on relevant regulations and be prepared to discuss how you've navigated these in past roles, as this will show your readiness for the responsibilities of the position.
