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For Companies At a Glance
- Tasks: Lead innovative clinical trial designs and contribute to impactful regulatory submissions.
- Company: Join a leading biopharmaceutical company dedicated to improving patient outcomes.
- Benefits: Enjoy competitive benefits, professional development, and a supportive work environment.
- Other info: Collaborative culture with opportunities for global travel and career growth.
- Why this job: Make a real difference in healthcare by applying your statistical expertise.
- Qualifications: PhD or master's in statistics/biostatistics with 3+ years in drug development.
The predicted salary is between 60000 - 80000 £ per year.
The biostatistician is a member of cross‑functional development teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. With appropriate experience, biostatisticians can have responsibilities for integrated summaries and/or supporting a particular indication of an asset.
Key Responsibilities
- Contributes to preparation of the development strategy that will allow for effective and safe utilization of the product.
- Drives the design of innovative and efficient clinical trials, including the selection of populations to study and endpoints to use, and develops trial designs that address study objectives that will support regulatory approval and market access.
- Translates scientific questions into statistical terms and statistical concepts into lay terms.
- Ensures that all analyses conducted have clearly articulated hypotheses associated with them and that the trial design and data collected support conducting the analysis.
- Communicates effectively with clinical and regulatory partners and external opinion leaders.
- Builds the external reputation of BMS through collaborations with alliance partners, academic and government research organizations, and conference participation.
- Authors and/or reviews protocol synopsis, protocol, statistical analysis plan, data presentation plan, case‑report forms, clinical study reports, associated publications, and other study‑level specification documents.
- Exercises cost‑disciplined science in sizing of the trials and in planning for the analyses to be conducted.
- Complies with BMS processes and SOPs, global and project standards, and is responsible for the quality of statistical deliverables, e.g., tables, listings, and figures.
- Takes accountability for ensuring quality in all planning, design, and execution of the assigned protocol or project.
- Collaborates with clinicians and medical writers to prepare summaries of results for use in regulatory documents and scientific articles.
- Drives, with the clinician, the interpretation of results, development of key messages, and communication to the development team.
- Drives alignment at the team level and escalates lack of alignment to the GBDS Lead for resolution.
- Provides statistical consultation for ad hoc analysis requests, including design of appropriate analyses to answer relevant questions.
- Keeps up to date with state‑of‑the‑art applied statistical methodology.
Qualifications & Experience
- Significant academic training in statistics, biostatistics, or relevant areas of study.
- PhD degree in statistics or biostatistics or a master’s degree with relevant experience required.
- More than 3 years of pharmaceutical/drug development or other related experience.
- Understanding of the application of biostatistics to medical/clinical trials data.
- Ability to work successfully within cross‑functional teams leading to successful global regulatory filings and approvals.
- Excellent verbal and written communication skills.
- Ability to organize multiple work assignments and establish priorities.
- May require up to 20% domestic and/or international business travel.
Benefits & Opportunities
BMS offers competitive benefits, services, and programs to support employees in their professional and personal lives.
Equal Employment Opportunity
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Senior Manager, Biostatistics in London employer: Bristol Myers Squibb
Contact Detail:
Bristol Myers Squibb Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Manager, Biostatistics in London
✨Network Like a Pro
Get out there and connect with people in the biostatistics field! Attend conferences, join relevant online forums, and engage with professionals on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Show Off Your Skills
When you get the chance to chat with potential employers, make sure to highlight your experience in trial design and statistical analysis. Use specific examples from your past work to demonstrate how you've contributed to successful projects. This will help you stand out as a candidate who can drive results.
✨Prepare for Interviews
Before any interview, brush up on common biostatistics concepts and be ready to discuss how they apply to clinical trials. Practice articulating your thoughts clearly, especially when translating complex statistical ideas into layman's terms. This will show that you can communicate effectively with both technical and non-technical team members.
✨Apply Through Our Website
Don't forget to check out our website for the latest job openings at StudySmarter! Applying directly through our site not only streamlines the process but also shows your genuine interest in joining our team. Plus, we love seeing familiar names pop up in our applications!
We think you need these skills to ace Senior Manager, Biostatistics in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the specific skills and experiences mentioned in the job description. Highlight your biostatistics expertise and any relevant projects you've worked on that align with the responsibilities of the Senior Manager role.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you're the perfect fit for this position. Share your passion for biostatistics and how your background can contribute to innovative clinical trial designs and regulatory submissions.
Showcase Your Communication Skills: Since effective communication is key in this role, make sure your application demonstrates your ability to translate complex statistical concepts into lay terms. This will show us you can collaborate well with cross-functional teams.
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 gives you a chance to explore more about our company culture!
How to prepare for a job interview at Bristol Myers Squibb
✨Know Your Stats
Brush up on your biostatistics knowledge and be ready to discuss how you've applied statistical methods in clinical trials. Be prepared to translate complex statistical concepts into layman's terms, as this will showcase your ability to communicate effectively with cross-functional teams.
✨Understand the Role
Familiarise yourself with the key responsibilities outlined in the job description. Think about how your past experiences align with these tasks, especially in trial design and regulatory submissions. This will help you demonstrate that you're not just a fit for the role, but that you can excel in it.
✨Prepare for Scenario Questions
Expect scenario-based questions that assess your problem-solving skills and decision-making process. Prepare examples from your previous work where you drove trial designs or collaborated with clinicians, highlighting your contributions and the outcomes.
✨Showcase Your Communication Skills
Since effective communication is crucial for this role, practice articulating your thoughts clearly and concisely. You might be asked to explain a complex analysis or result, so being able to convey your ideas simply will set you apart from other candidates.