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For Companies At a Glance
- Tasks: Lead programming projects and generate insightful data from clinical trials using SAS.
- Company: Join a leading pharmaceutical company focused on innovation and excellence.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact in the healthcare industry while advancing your career.
- Qualifications: Master's degree and 5+ years in Statistical Programming required.
- Other info: Collaborative environment with a focus on problem-solving and communication.
The predicted salary is between 36000 - 60000 £ 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) in London 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) in London
✨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, especially those involving SDTM and ADaM standards. 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 clinical trials and statistical programming. Brush up on your knowledge of ICH guidelines and be ready to discuss how you’ve tackled challenges in past projects.
✨Tip Number 4
Don’t forget to apply through our website! We’re always on the lookout for talented individuals like you. Plus, it’s a great way to ensure your application gets seen by the right people.
We think you need these skills to ace Senior Statistical Programmer - UK (Remote) in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your mastery in SAS programming and experience with clinical trial databases. We want to see how your skills align with the job description, so don’t be shy about showcasing your relevant experience!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for the Senior Statistical Programmer role. Mention your advanced knowledge of E-Submission Standards and any leadership experience you have in programming projects.
Showcase Problem-Solving Skills: We love candidates who can think on their feet! In your application, give examples of how you've tackled challenges in statistical programming or clinical trials. This will demonstrate your excellent problem-solving skills and ability to work collaboratively.
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 shows you’re keen on joining the StudySmarter team!
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 SAS Macros, as this will show your mastery of the tools required for the role.
✨Understand the SDLC
Familiarise yourself with the System Development Life Cycle (SDLC) as it relates to programming deliverables. Be prepared to explain how you've applied this framework in past projects, highlighting your ability to manage programming tasks effectively.
✨Get Acquainted with E-Submission Standards
Review the E-Submission Standards, Guidelines, and Regulations, particularly focusing on SDTM and ADaM standards. You might be asked to write specifications during the interview, so having examples ready will demonstrate your advanced knowledge and readiness for the role.
✨Showcase Your Leadership Skills
Since the role involves leading study or small programming project teams, think of instances where you've taken charge. Discuss your approach to problem-solving and how you communicate with team members to ensure everyone is aligned and working towards common goals.
