At a Glance
- Tasks: Transform complex clinical data into clear, submission-ready outputs for regulatory approval.
- Company: Join Bristol Myers Squibb, a leader in biopharma innovation.
- Benefits: Impactful work, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on mentorship and team development.
- Why this job: Make a real difference in patient outcomes through your programming expertise.
- Qualifications: 7+ years in statistical programming with strong SAS and CDISC knowledge.
The predicted salary is between 70000 - 90000 € per year.
At Bristol Myers Squibb you will be the programming expert that clinical project teams rely on, transforming complex, messy clinical data into clear, submission‑ready outputs that regulators trust. You will design and implement technical solutions that directly influence whether a medicine moves forward – or doesn’t. Your expertise in CDISC standards, ADaM specifications, SAS programming, and electronic submissions will have a direct line to patient outcomes. You will be embedded in cross‑functional teams, partnering with statisticians, data managers, clinical scientists, and external vendors within BMS’ Global Biometrics & Data Sciences (GBDS) organization and beyond.
Responsibilities
- Analyze, clean, and transform clinical data for regulatory submissions, ensuring compliance with CDISC standards.
- Develop and maintain SAS programs for ADaM datasets and analysis tables.
- Prepare electronic submission components and coordinate e‑submission workflows with appropriate teams.
- Review statistical analysis plans, shape programming strategy, and advise senior stakeholders on risk and resolution.
- Drive process improvements and lead initiatives to increase efficiency across statistical programming practices.
- Collaborate with various functional groups—statisticians, data managers, clinical scientists, and vendors—to streamline work streams.
Qualifications
- 7+ years of statistical programming experience in the pharmaceutical or biopharma industry, including hands‑on involvement in major regulatory submissions.
- Deep fluency in SAS, CDISC/SDTM/ADaM standards, and the end‑to‑end clinical data pipeline.
- Understanding of the full drug development lifecycle – from eDC data collection through to TFLs and e‑submission components.
- Strong communication skills; able to hold your own in a room of statisticians, clinicians, and regulatory experts.
- Proactive about spotting problems before they become crises and confident enough to communicate them clearly.
- Hold a degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences.
On-site Protocol
BMS determines where an employee is required to conduct their work based on occupancy type (site‑essential, site‑by‑design, field‑based, remote‑by‑design). Site‑essential roles require 100% of shifts onsite. Site‑by‑design roles may allow a hybrid model with at least 50% onsite.
Supporting People With Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations, and ongoing support. Applicants can request accommodations prior to accepting a job offer.
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Senior Manager, Statistical Programming in Uxbridge employer: Bristol Myers Squibb
At Bristol Myers Squibb, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. As a Senior Manager in Statistical Programming, you will have the opportunity to make a real impact on patient outcomes while working alongside talented professionals in a supportive environment that encourages growth and development. With a commitment to driving change and improving processes, you'll be empowered to lead initiatives that enhance our statistical programming practices, all while contributing to groundbreaking clinical trials that redefine standard care worldwide.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Manager, Statistical Programming in Uxbridge
✨Network Like a Pro
Get out there and connect with folks in the industry! Attend conferences, webinars, or local meetups related to statistical programming. The more people you know, the better your chances of hearing about job openings before they even hit the market.
✨Show Off Your Skills
When you get the chance to chat with potential employers, don’t hold back! Share specific examples of how you've transformed complex data into clear outputs. Highlight your experience with CDISC standards and SAS programming to show you're the expert they need.
✨Tailor Your Approach
Every company is different, so make sure you tailor your conversations to fit their needs. Research Bristol Myers Squibb and understand their projects and values. This way, you can align your skills and experiences with what they’re looking for.
✨Apply Through Our Website
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining the team at BMS and making a real impact in the field.
We think you need these skills to ace Senior Manager, Statistical Programming in Uxbridge
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to highlight your experience in statistical programming and regulatory submissions. We want to see how your skills align with the job description, so don’t be shy about showcasing your SAS expertise and knowledge of CDISC standards!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about the role and how your background makes you the perfect fit. We love seeing candidates who can connect their experiences to the impact they can have on patient outcomes.
Showcase Your Teamwork Skills:Since collaboration is key in this role, make sure to highlight any experience you have working in cross-functional teams. We want to know how you’ve partnered with statisticians, data managers, and other professionals to drive successful projects.
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensure it gets into the right hands. Plus, it shows you’re serious about joining our team at Bristol Myers Squibb!
How to prepare for a job interview at Bristol Myers Squibb
✨Know Your Stuff
Make sure you brush up on your SAS programming skills and CDISC standards. Be ready to discuss how you've applied these in past projects, especially in regulatory submissions. This will show that you’re not just familiar with the concepts but have real-world experience.
✨Showcase Your Collaboration Skills
Since this role involves working with cross-functional teams, prepare examples of how you've successfully collaborated with statisticians, data managers, and clinical scientists. Highlight any specific projects where teamwork led to improved outcomes or efficiencies.
✨Prepare for Technical Questions
Expect technical questions related to ADaM specifications and the end-to-end clinical data pipeline. Practise explaining complex concepts in simple terms, as you'll need to communicate effectively with various stakeholders during your role.
✨Demonstrate Problem-Solving Abilities
Be ready to discuss instances where you identified potential issues before they escalated. Share how you approached these challenges and the solutions you implemented. This will showcase your proactive mindset and ability to handle pressure.
