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 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, 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 Belfast employer: MMS
MMS is an award-winning clinical research organization that values your contributions and fosters a supportive, innovative work culture. With a Great Place to Work certification and a commitment to employee growth, we offer exceptional opportunities for career advancement in a collaborative environment. Join us remotely in the UK and be part of a team that is shaping the future of clinical research while enjoying industry-leading benefits and a focus on work-life balance.
StudySmarter Expert Advice🤫
We think this is how you could land Remote Senior Statistical Programmer - UK (Remote) in Belfast
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work at MMS or similar companies. A friendly chat can open doors and give you insights that might just land you an interview.
✨Tip Number 2
Prepare for the interview by brushing up on your SAS skills and understanding the latest in clinical trial regulations. We want to see your expertise shine, so be ready to discuss your experience with SDTM and ADaM standards!
✨Tip Number 3
Show us your problem-solving skills! During interviews, be prepared to tackle hypothetical scenarios related to statistical programming. This is your chance to demonstrate how you approach challenges and find solutions.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, you’ll get a feel for our company culture and values right from the start.
We think you need these skills to ace Remote Senior Statistical Programmer - UK (Remote) in Belfast
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. We love seeing genuine enthusiasm!
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 value problem solvers who can think on their feet and contribute to our innovative environment.
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 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 faced and how you overcame them, as this demonstrates your problem-solving abilities.
✨Communicate Clearly and Confidently
Good communication is key in this role. Practice articulating your thoughts clearly and concisely, especially when discussing complex statistical concepts. Remember, it's not just about what you know, but how you convey that knowledge to others.
