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- 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 strong problem-solving and communication skills.
- Other info: Be part of a supportive environment that values your career development.
The predicted salary is between 36000 - 60000 £ per year.
Director Clinical Operations and Biometrics, Global Biometrics SME
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.
- 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.
Qualifications
- 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.
Seniority level
- Mid-Senior level
Employment type
- Full-time
Job function
- Science
Industries
- Professional Services
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Principal Statistical Programmer - FSP employer: Proclinical Staffing
Contact Detail:
Proclinical Staffing 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 land you that dream job.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to statistical programming. We recommend doing mock interviews with friends or using online resources to boost your confidence and refine your answers.
✨Tip Number 3
Showcase your skills! Create a portfolio of your work, including any SAS programs or projects you've led. This will give potential employers a tangible sense of your expertise and how you can contribute to their team.
✨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, we’re always here to help if you have any questions during the process.
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. Don’t just list your duties; show how you’ve made an impact in previous roles!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for this role. Mention specific projects or experiences that relate to the responsibilities listed in the job description. We want to see your passion for statistical programming!
Showcase Your Leadership Skills: Since this role involves people management, make sure to highlight any leadership experience you have. Talk about how you've mentored others or led projects. We value collaboration and innovation, so let us know how you foster these in your teams!
Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It’s quick and easy, and ensures your application gets to the right place. Plus, we love seeing candidates who take the initiative to apply directly!
How to prepare for a job interview at Proclinical Staffing
✨Know Your SAS Inside Out
Make sure you brush up on your SAS programming skills before the interview. Be prepared to discuss your experience with clinical trial disclosures and data anonymisation, as these are key aspects of the role. Practising coding challenges or reviewing past projects can help you articulate your technical expertise.
✨Familiarise Yourself with CDISC Standards
Since familiarity with CDISC standards is crucial for this position, take some time to review SDTM and ADaM guidelines. Being able to discuss how you've applied these standards in previous roles will show your depth of knowledge and commitment to high-quality deliverables.
✨Showcase Your Leadership Skills
This role involves mentoring and managing a team, so be ready to share examples of how you've led projects or supported colleagues in their development. Highlighting your communication skills and ability to foster collaboration will demonstrate that you're not just a technical expert but also a great team player.
✨Prepare for Scenario-Based Questions
Expect to face scenario-based questions that assess your problem-solving abilities and decision-making process. Think about past challenges you've encountered in statistical programming and how you resolved them. This will help you convey your analytical thinking and adaptability during the interview.
