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 Derry 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 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 Derry
✨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 virtual interview! Research common questions for Senior Statistical Programmers and practice your answers. We want to see your expertise shine, so be ready to discuss your experience with SAS and clinical trials.
✨Tip Number 3
Show off your skills! If you have any projects or case studies that highlight your mastery of SDTM standards or ADaM standards, bring them up during your conversations. Real examples can make you stand out!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re genuinely interested in joining our awesome team at MMS.
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 great fit for the role.
Craft a Compelling Cover Letter:Use your cover letter to tell us why you’re passionate about clinical research and how your background aligns with our mission at MMS. Share specific examples of your achievements in statistical programming to make your application stand out.
Showcase Your Problem-Solving Skills:In your application, don’t forget to mention instances where you've tackled complex challenges in your previous roles. We love candidates who can demonstrate their problem-solving abilities, especially in a collaborative environment like ours.
Apply Through Our Website:We encourage you to submit your application through our website. This way, you’ll ensure that your application gets to the right people and you’ll be one step closer to joining our innovative team at MMS!
