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 development.
- 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 Newtownabbey employer: MMS
At MMS, we are committed to creating a workplace where your expertise as a Senior Statistical Programmer is valued and nurtured. Our Great Place to Work certification reflects our dedication to fostering a supportive and innovative culture, offering exceptional employee retention rates and opportunities for professional growth. Join us in our remote UK team and be part of a collaborative environment that not only prioritises your career advancement but also shapes the future of clinical research.
StudySmarter Expert Advice🤫
We think this is how you could land Remote Senior Statistical Programmer - UK (Remote) in Newtownabbey
✨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 insider info on job openings.
✨Tip Number 2
Prepare for virtual interviews by practising common questions and showcasing your SAS programming skills. We want to see how you tackle real-world problems, so be ready to share examples from your experience.
✨Tip Number 3
Show off your passion for clinical research! When you get the chance, talk about why you love this field and how your expertise aligns with MMS's mission. It’s all about making that personal connection.
✨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 find all the latest opportunities right there, tailored just for you.
We think you need these skills to ace Remote Senior Statistical Programmer - UK (Remote) in Newtownabbey
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 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, it shows you’re keen on joining our team!
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
Since the role involves leading study or small programming project teams, think of examples where you've taken charge. Highlight your ability to collaborate and communicate effectively with team members to solve problems and meet project goals.
✨Prepare Questions for Them
Interviews are a two-way street! Prepare thoughtful questions about MMS's culture, their approach to clinical research, and how they support employee growth. This shows your genuine interest in the company and helps you assess if it's the right fit for you.
