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For Companies At a Glance
- Tasks: Lead programming projects and generate insightful data visuals from clinical trial databases.
- Company: Join a leading pharmaceutical company focused on innovation and excellence.
- Benefits: Enjoy remote work, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact in the healthcare industry with your statistical expertise.
- Qualifications: Master's degree and 5+ years in Statistical Programming required.
- Other info: Collaborative environment with a focus on continuous learning and development.
The predicted salary is between 48000 - 72000 £ per year.
Job Specific Skills:
- Mastery and trained on generating tables, listings, and graphs from clinical trial databases using SAS.
- Utilizes System Development Life Cycle (SDLC) for programming deliverables.
- Advanced user in SAS programming, SAS Base, and SAS Macros.
- Advanced knowledge of E-Submission Standards, Guidelines and Regulations.
- Mastery and trained on SDTM standards including ability to write specifications.
- Advanced knowledge of ADaM standards including supporting specification writing.
- Proficient with MS Office applications.
- Advanced knowledge of ICH, 21CRF Part 11, and ISO 9001:2000 requirements.
- Advanced experience with pooling of data sets for submissions.
- Advanced experience with BIMO outputs, define.xml, Reviewer’s Guides, SDSP.
- Lead study or small programming project teams.
Job Requirements:
- Masters required for all Statistics roles.
- Minimum of 5 years’ experience in Statistical Programming or similar field required.
- Expert knowledge of scientific principles and concepts.
- Reputation as emerging leader in field with sustained performance and accomplishment.
- Proficiency with MS Office applications.
- Hands-on experience with clinical trial and pharmaceutical development preferred.
- Good communication skills and willingness to work with others to clearly understand needs and solve problems.
- Excellent problem-solving skills.
- Good organizational and communication skills.
- Familiarity with current ISO 9001 and ISO 27001 standards preferred.
- Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
- Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.
Senior Statistical Programmer - UK (Remote) employer: MMS Holdings Inc.
Contact Detail:
MMS Holdings Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Statistical Programmer - UK (Remote)
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work in statistical programming or clinical trials. A friendly chat can lead to insider info about job openings that aren’t even advertised yet.
✨Tip Number 2
Show off your skills! Prepare a portfolio showcasing your SAS programming projects, tables, and graphs you've generated. This will give potential employers a clear view of what you can bring to the table.
✨Tip Number 3
Ace the interview by preparing for common questions related to SDTM and ADaM standards. Brush up on your knowledge of ICH guidelines and be ready to discuss how you’ve applied these in past roles.
✨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 love seeing candidates who are proactive about their job search!
We think you need these skills to ace Senior Statistical Programmer - UK (Remote)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Statistical Programmer role. Highlight your mastery in SAS programming and any relevant experience with clinical trial databases. We want to see how your skills align with what we're looking for!
Showcase Your Experience: When writing your application, don’t just list your past jobs. Instead, showcase specific projects where you’ve led teams or tackled complex programming challenges. This helps us see your problem-solving skills in action!
Be Clear and Concise: Keep your written application clear and to the point. Use bullet points for key achievements and avoid jargon unless it’s relevant. We appreciate straightforward communication that gets to the heart of your experience.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of applications and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at MMS Holdings Inc.
✨Know Your SAS Inside Out
Make sure you brush up on your SAS programming skills, especially in generating tables, listings, and graphs from clinical trial databases. Be ready to discuss specific projects where you've used SAS Base and Macros, as well as how you've applied SDTM and ADaM standards.
✨Familiarise Yourself with Regulations
Since the role requires advanced knowledge of ICH, 21 CFR Part 11, and ISO standards, take some time to review these regulations. Prepare to explain how you've implemented these guidelines in your previous work, as this will show your understanding of compliance in statistical programming.
✨Showcase Your Leadership Skills
As an emerging leader in your field, be prepared to share examples of how you've led study or programming project teams. Highlight your problem-solving skills and how you've effectively communicated with team members to achieve project goals.
✨Prepare for Technical Questions
Expect technical questions related to the System Development Life Cycle (SDLC) and data pooling for submissions. Practise articulating your thought process and methodologies clearly, as this will demonstrate your expertise and ability to tackle complex programming challenges.
