At a Glance
- Tasks: Join a supportive team to analyse clinical trial data and lead programming projects.
- Company: Award-winning CRO known for its exceptional culture and employee satisfaction.
- Benefits: Flexible remote work, competitive salary, and opportunities for professional growth.
- Other info: Be part of a global team shaping the future of healthcare.
- Why this job: Make a real impact in clinical research while advancing your career in a collaborative environment.
- Qualifications: Master's degree and 5+ years in Statistical Programming with SAS expertise.
The predicted salary is between 60000 - 80000 £ per year.
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Senior Statistical Programmer 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.
Remote Senior Statistical Programmer - UK (Remote) in Stirling employer: MMS
MMS is an exceptional employer that values your contributions and fosters a supportive, innovative work culture. As a Great Place to Work certified organisation, we offer outstanding employee retention rates and numerous growth opportunities within the dynamic field of clinical research. Join our collaborative team and enjoy the benefits of working remotely in the UK, where you can thrive while shaping the future of healthcare.
StudySmarter Expert Advice🤫
We think this is how you could land Remote Senior Statistical Programmer - UK (Remote) in Stirling
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend virtual meetups, and engage with professionals on LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for those interviews! Research MMS thoroughly, understand their values, and be ready to discuss how your skills align with their mission. We want to see your passion for clinical research and how you can contribute to our innovative team.
✨Tip Number 3
Showcase your expertise! Bring examples of your previous work, especially any SAS programming projects or clinical trial data analyses you've done. We love seeing how you’ve tackled challenges and delivered results in your past roles.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for talented individuals who are eager to join our supportive and collaborative environment at MMS.
We think you need these skills to ace Remote Senior Statistical Programmer - UK (Remote) in Stirling
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior Statistical Programmer role. Highlight your experience with SAS programming and any relevant projects you've led. We want to see how your skills align with our needs!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Share your passion for clinical research and how you can contribute to our innovative team. Let us know why you're excited about joining MMS and what makes you a great fit.
Showcase Your Achievements:Don’t just list your responsibilities; showcase your achievements! Use specific examples of how you've tackled challenges in statistical programming or led successful projects. We love to see results!
Apply Through Our Website:We encourage you to apply through our website for a smoother process. It’s the best way for us to receive your application and get you on our radar. Plus, you’ll find all the details about the role there!
How to prepare for a job interview at MMS
✨Know Your SAS Inside Out
Make sure you brush up on your SAS programming skills, especially in generating tables, listings, and graphs. Be prepared to discuss specific projects where you've used SAS Base and Macros, as well as your experience with SDTM and ADaM standards.
✨Understand the Regulatory Landscape
Familiarise yourself with ICH guidelines, 21 CFR Part 11, and ISO standards relevant to the role. Being able to articulate how these regulations impact statistical programming will show that you’re not just technically skilled but also aware of the broader context.
✨Showcase Your Leadership Skills
If you've led study or programming project teams, be ready to share examples. Highlight your ability to collaborate and communicate effectively with team members, as this is crucial in a supportive environment like MMS.
✨Prepare Thoughtful Questions
Think of insightful questions to ask about the company culture and the specific challenges they face in clinical research. This shows your genuine interest in the role and helps you determine if MMS is the right fit for you.
