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For Companies At a Glance
- Tasks: Lead statistical programming for clinical studies and collaborate with cross-functional teams.
- Company: Join Novartis, a leader in the pharmaceutical industry with a passion for innovation.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Why this job: Make a real impact on drug development and improve patient outcomes.
- Qualifications: Experience in statistical programming, particularly with SAS, and strong communication skills.
- Other info: Dynamic work environment with opportunities for career advancement.
The predicted salary is between 54000 - 84000 £ per year.
We have an exciting opportunity for a Senior Principal Statistical Programmer, to join a passionate team within Advanced Quantitative Sciences – Development. Come to an industry leader where you will be responsible for all statistical programming aspects of several studies, a medium to large sized project or project-level activities (incl. submission and post‑marketing activities). The position is a key collaborator and strategic partner with biostatistics in ensuring that pharmaceutical drug‑development plans in Novartis Global Drug Development are executed efficiently with timely and high‑quality deliverables.
About the role
- Lead statistical programming activities as Trial Programmer for several studies or as Lead/Program Programmer for a medium to large sized project in phase I to IV clinical studies in Novartis Global Development Organization.
- Co‑ordinate activities of programmers either internally or externally.
- Make statistical programming decisions and propose strategies at study or project level.
- May act as functional manager for local associates including providing supervision and advice to these programmers on functional expertise and processes.
- Build and maintain effective working relationship with cross‑functional teams, able to summarize and discuss status of deliverables and critical programming aspects (timelines, scope, resource plan), e.g. as SP representative in study‑ or project‑level team.
- Review eCRF, discuss data structures and review activities, ensure project‑level standardization which allows pooling and efficient CRT production.
- Comply with company, department and industry standards (e.g. CDISC) and processes, assess and clarify additional programming requirements, review, develop and influence programming specifications as part of the analysis plans (incl. CSPD and other project‑level strategies).
- Provide and implement statistical programming solutions; ensure knowledge sharing.
- Act as programming expert in problem‑solving aspects.
- Ensure timely and quality development and validation of datasets and outputs for CSRs, regulatory submissions/interactions, safety reports, publications, post‑marketing activities or exploratory analyses (as required) in the assigned drug development studies/project.
- Responsible for quality control and audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results.
- Maintain up‑to‑date advanced knowledge of programming software (e.g. SAS) as well as industry requirements (e.g. CDISC SDTM/ADaM, eCTD, Define.xml), attend functional meetings and trainings.
- Establish successful working relationship on individual studies with external associates according to agreed contract and internal business guidance.
- Act as subject matter expert (SME) or, as assigned, lead process improvement/non‑clinical project initiatives with a focus on programming and analysis reporting procedures.
Experience
- BA/BS/MS or international equivalent experience in statistics, computer science, mathematics, life sciences or related field.
- Work experience in a programming role preferably supporting clinical trials or in pharmaceutical industry.
- Expert SAS experience and proven skills in the use of SAS within a Statistical Programming environment to develop and validate deliverables, proven experience in development of advanced MACROs.
- Advanced experience in contributing to statistical analysis plans and/or constructing technical programming specifications.
- Advanced knowledge of industry standards including CDISC data structures as well as a solid understanding of the development and use of standard programs.
- Good understanding of regulatory requirements relevant to Statistical Programming (e.g. GCP, study procedures).
- Proven communications and negotiation skills, ability to work well with others globally and influence.
- Experience as Trial/Lead/Project Programmer for several studies or project-level activities, including coordination of team of internal or external programmers on a given study/project, ability to transfer own knowledge to others.
How to Apply
To find out more and apply, please click here.
Novartis - Senior Principal Statistical Programmer in Sheffield employer: Promoting Statistical Insights
Contact Detail:
Promoting Statistical Insights Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Novartis - Senior Principal Statistical Programmer in Sheffield
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work at Novartis or similar companies. A friendly chat can sometimes lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your technical skills and industry knowledge. Make sure you can confidently discuss your experience with SAS and statistical programming, as well as how you've contributed to successful projects in the past.
✨Tip Number 3
Showcase your problem-solving skills! Be ready to share examples of how you've tackled challenges in previous roles, especially in a clinical trial setting. This will demonstrate your ability to think critically and adapt in a fast-paced environment.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you're genuinely interested in joining our team at Novartis.
We think you need these skills to ace Novartis - Senior Principal Statistical Programmer in Sheffield
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Principal Statistical Programmer role. Highlight your experience with SAS and any relevant projects you've worked on, especially in clinical trials. We want to see how your skills align with what we're looking for!
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 background makes you a great fit for our team. Don't forget to mention your experience with CDISC standards and any leadership roles you've had.
Showcase Your Problem-Solving Skills: In your application, be sure to highlight specific examples where you've solved complex programming issues or improved processes. We love seeing candidates who can think critically and bring innovative solutions to the table!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, you'll find all the details you need about the role and our company culture there!
How to prepare for a job interview at Promoting Statistical Insights
✨Know Your Stats Inside Out
Make sure you brush up on your statistical programming knowledge, especially with SAS. Be ready to discuss your experience with developing and validating deliverables, as well as any advanced MACROs you've created. This will show that you're not just familiar with the tools, but that you can use them effectively in a clinical trial setting.
✨Understand the Role of Collaboration
Since this position involves working closely with biostatistics and cross-functional teams, be prepared to share examples of how you've successfully collaborated in the past. Highlight your communication skills and how you've influenced project outcomes through teamwork. This will demonstrate that you can build effective working relationships.
✨Familiarise Yourself with Industry Standards
Get to grips with CDISC standards and regulatory requirements relevant to statistical programming. Being able to discuss these standards confidently will show that you understand the importance of compliance and quality control in drug development, which is crucial for this role.
✨Prepare for Problem-Solving Scenarios
Think about potential challenges you might face in statistical programming and how you would approach solving them. Be ready to discuss specific examples from your past experiences where you acted as a subject matter expert or led process improvements. This will highlight your problem-solving skills and your ability to think strategically.