At a Glance
- Tasks: Join a supportive team to analyse clinical trial data and drive impactful research.
- 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: 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 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 Wrexham 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 Wrexham
✨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 in SAS programming and statistical analysis can contribute to their innovative projects. We want to see your passion shine through!
✨Tip Number 3
Showcase your expertise! Create a portfolio or a GitHub repository where you can display your programming projects, especially those related to clinical trials. This gives us a tangible way to see your skills in action and how you tackle real-world problems.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us. Let’s make this happen together!
We think you need these skills to ace Remote Senior Statistical Programmer - UK (Remote) in Wrexham
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 what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your background makes you a great fit for our team. Let us know what excites you about working at MMS.
Showcase Your Problem-Solving Skills:In your application, don’t forget to mention specific examples of how you've tackled challenges in your previous roles. We love seeing candidates who can think critically and solve problems effectively!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, you’ll get to explore more about our amazing culture!
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 ready to discuss specific projects where you've used SAS Base and Macros, as well as how you've applied SDTM and ADaM standards in your work.
✨Understand the Regulatory Landscape
Familiarise yourself with ICH guidelines, 21 CFR Part 11, and ISO standards relevant to clinical research. Prepare to explain how you've navigated these regulations in past roles, 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 ready to share examples of your leadership style and how you foster collaboration. Highlight any experiences where you've successfully guided a team through challenges, as this aligns with MMS's supportive culture.
✨Communicate Clearly and Confidently
Good communication is key in this role. Practice articulating complex statistical concepts in simple terms, as you'll need to work closely with others. Think of examples where you've solved problems collaboratively, showcasing your ability to understand and meet team needs.
