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: Shape the future of medicine and improve patient outcomes through your expertise.
- Qualifications: 7+ years in statistical programming with strong SAS and CDISC knowledge.
The predicted salary is between 60000 - 80000 € 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 London employer: Bristol Myers Squibb
At Bristol Myers Squibb, we pride ourselves on being an exceptional employer that values innovation and collaboration. Our work culture fosters a sense of purpose, where you can make a real impact on patient outcomes through your expertise in statistical programming. With ample opportunities for professional growth, mentorship, and the chance to lead initiatives that drive efficiency, you'll find a rewarding environment that supports your career aspirations while working alongside dedicated professionals in the heart of the biopharma industry.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Manager, Statistical Programming in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those at Bristol Myers Squibb. A friendly chat can sometimes lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your SAS programming skills and CDISC standards. Be ready to discuss how you’ve tackled complex data challenges in the past – real examples will make you stand out!
✨Tip Number 3
Show off your collaborative spirit! Highlight experiences where you’ve worked with cross-functional teams. At BMS, they value teamwork, so let them know you’re all about driving success together.
✨Tip Number 4
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 Bristol Myers Squibb.
We think you need these skills to ace Senior Manager, Statistical Programming in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to highlight your experience with SAS programming and CDISC standards. We want to see how your skills align with the role, so don’t be shy about showcasing your relevant projects!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about statistical programming and how your expertise can make a difference at Bristol Myers Squibb. Let us know what excites you about the role!
Showcase Your Teamwork Skills:Since collaboration is key in this role, highlight any experiences where you’ve worked with cross-functional teams. We love to see how you’ve partnered with statisticians, data managers, or clinical scientists in the past.
Apply Through Our Website:Don’t forget to apply 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 to navigate!
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 statistical programming and data transformation. Practice explaining complex concepts in simple terms, as you'll need to communicate effectively with both technical and non-technical stakeholders.
✨Demonstrate Problem-Solving Abilities
Be ready to discuss how you've identified and resolved issues in previous roles. Think of specific examples where your proactive approach made a difference, especially in high-stakes situations like regulatory submissions.
