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For Companies At a Glance
- Tasks: Lead statistical programming projects and mentor a dynamic team in the pharmaceutical industry.
- Company: Join a leading life sciences recruiter with a focus on innovation and collaboration.
- Benefits: Enjoy remote work flexibility, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact in clinical trials while developing your leadership skills.
- Qualifications: Proficient in SAS programming with a background in clinical trials and strong problem-solving abilities.
- Other info: Be part of a supportive environment that values your career development.
The predicted salary is between 36000 - 60000 £ per year.
Overview
Shape your future with the freedom to work where you thrive! Join our pharmaceutical client with this remote role in Statistical Programming.
Proclinical is seeking a Principal Statistical Programmer to give support across a variety of projects, clients, and therapeutic areas. This role involves technical expertise, project oversight, and people management responsibilities. You will play a key role in ensuring high-quality deliverables while fostering collaboration and innovation within the team.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities
- Evaluate clinical trial documents such as protocols, SAPs, CRFs, and CSRs.
- Author, review, and approve study TFL shells and dataset specifications.
- Develop, validate, and document SAS programs for datasets, TFLs, and macros following best practices.
- Identify and resolve data issues, outliers, and standards discrepancies.
- Review and approve CDISC validation tool reports.
- Stay updated on emerging standards and their impact on trials.
- Maintain audit-ready study master file documents.
- Provide technical leadership and mentorship to team members.
- Line manage statisticians, programmers, and other technical staff, supporting their career development and training.
- Oversee client projects, including resource management, risk assessment, and delivery to budget.
- Lead internal and client meetings, share knowledge, and contribute to process improvement initiatives.
Key Skills and Requirements
- Proficiency in SAS programming with experience in clinical trial disclosures and/or data anonymization.
- Familiarity with CDISC standards (SDTM, ADaM) and TLF generation.
- Strong problem-solving skills and ability to apply anonymization criteria to study data.
- Excellent communication and leadership skills.
- Understanding of the clinical drug development process, study designs, and relevant disease areas.
- BSc, MSc, or PhD in a numerical discipline or equivalent industry experience.
If you are having difficulty in applying or if you have any questions, please contact Heidi Hennigan at h.hennigan@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click \’Apply\’ or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you\’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.proclinical.com/privacy-policy.
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Principal Statistical Programmer - FSP employer: Proclinical Group
Contact Detail:
Proclinical Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Statistical Programmer - FSP
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend virtual meetups, and engage on platforms like LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that Principal Statistical Programmer role.
✨Tip Number 2
Prepare for those interviews! Brush up on your SAS programming skills and be ready to discuss your experience with clinical trial documents. We recommend practising common interview questions and even doing mock interviews with friends or mentors to boost your confidence.
✨Tip Number 3
Showcase your leadership skills! As a Principal Statistical Programmer, you’ll need to demonstrate your ability to manage projects and mentor others. We suggest sharing specific examples from your past experiences where you’ve led a team or improved processes.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. We’re here to help you every step of the way, so if you have any questions, just reach out!
We think you need these skills to ace Principal Statistical Programmer - FSP
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Principal Statistical Programmer role. Highlight your SAS programming skills and experience with clinical trials, as these are key for us. Use specific examples that showcase your expertise in CDISC standards and data management.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Tell us why you're passionate about statistical programming and how your background aligns with our needs. Be sure to mention any leadership experience you have, as we value collaboration and mentorship.
Showcase Your Problem-Solving Skills: In your application, don’t forget to highlight your problem-solving abilities. We want to see how you've tackled data issues or discrepancies in the past. Share specific instances where your analytical skills made a difference in project outcomes.
Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity. Plus, it shows us you’re proactive!
How to prepare for a job interview at Proclinical Group
✨Know Your SAS Inside Out
Make sure you brush up on your SAS programming skills before the interview. Be prepared to discuss specific projects where you've developed, validated, or documented SAS programs. Highlight any experience with CDISC standards and how you've applied them in past roles.
✨Showcase Your Leadership Skills
As a Principal Statistical Programmer, you'll need to demonstrate your ability to lead and mentor others. Think of examples where you've successfully managed a team or contributed to their professional development. Be ready to discuss how you handle project oversight and resource management.
✨Familiarise Yourself with Clinical Trials
Understanding the clinical drug development process is crucial. Review key concepts related to clinical trial documents like protocols and SAPs. Be prepared to discuss how you've evaluated these documents in previous roles and any challenges you've faced.
✨Prepare for Problem-Solving Questions
Expect questions that assess your problem-solving abilities, especially regarding data issues and discrepancies. Think of specific instances where you've identified and resolved such issues, and be ready to explain your thought process and the outcomes.