At a Glance
- Tasks: Join a supportive team to analyse clinical trial data and drive impactful research.
- Company: Award-winning CRO known for its innovative culture and employee satisfaction.
- Benefits: Flexible remote work, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on innovation and employee well-being.
- Why this job: Make a real difference in clinical research while advancing your career.
- Qualifications: Master's degree and 5+ years in Statistical Programming required.
The predicted salary is between 50000 - 70000 £ 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, recognised 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.
- Utilises 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 organisational 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 Peterborough 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 opportunities for professional growth 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 making a meaningful impact in the pharmaceutical and biotech industries.
StudySmarter Expert Advice🤫
We think this is how you could land Remote Senior Statistical Programmer - UK (Remote) in Peterborough
✨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 along examples of your previous work, especially any SAS programming projects or statistical analyses you've led. 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 make a difference in the world of clinical research.
We think you need these skills to ace Remote Senior Statistical Programmer - UK (Remote) in Peterborough
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the specific skills and experiences mentioned in the job description. Highlight your mastery in SAS programming and any relevant projects you've led, as this will show us you're a perfect fit for the role.
Craft a Compelling Cover Letter:Use your cover letter to tell us why you want to join MMS and how your background aligns with our mission. Share your passion for clinical research and any innovative ideas you have that could contribute to our team.
Showcase Your Problem-Solving Skills:In your application, give examples of how you've tackled challenges in previous roles. We love seeing candidates who can think critically and come up with effective solutions, especially in the fast-paced world of clinical trials.
Apply Through Our Website:We encourage you to submit your application through our website. This way, you’ll ensure it reaches the right people directly, and you can easily keep track of your application status. Plus, it’s super straightforward!
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 from clinical trial databases. Be ready 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. Prepare to explain how you've applied these regulations in your previous work, as this will show your depth of knowledge and commitment to compliance.
✨Showcase Your Leadership Skills
If you've led study or programming project teams, be prepared to share examples of your leadership style and how you foster collaboration. Highlight any challenges you've faced and how you overcame them, as this demonstrates your problem-solving abilities.
✨Communicate Clearly and Confidently
Good communication is key in this role, so practice articulating your thoughts clearly. Think about how you can convey complex statistical concepts in a straightforward manner, as this will be crucial when working with cross-functional teams.
