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- Tasks: Lead programming projects and generate insightful data from clinical trials using SAS.
- Company: Join a leading biometrics company with a focus on innovation and collaboration.
- Benefits: Enjoy remote work, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact in the pharmaceutical industry while advancing your career.
- Qualifications: Master's degree and 5+ years in Statistical Programming required.
- Other info: Dynamic team environment with a chance to lead and innovate.
The predicted salary is between 36000 - 60000 £ per year.
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 & clinical data/terminology, & the drug development process.
Senior Statistical Programmer - UK (Remote) Biometrics BELFAST, NORTHERN IRELAND, UNITED KINGDOM employer: MMS Holdings Inc
Contact Detail:
MMS Holdings Inc Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Statistical Programmer - UK (Remote) Biometrics BELFAST, NORTHERN IRELAND, UNITED KINGDOM
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work in clinical trials or statistical programming. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Show off your skills! Create a portfolio showcasing your SAS programming projects, tables, and graphs. This will give potential employers a taste of what you can do and set you apart from the competition.
✨Tip Number 3
Prepare for interviews by brushing up on your knowledge of SDTM and ADaM standards. Be ready to discuss how you've applied these in past roles, as well as your experience with regulatory requirements like ICH and 21 CFR Part 11.
✨Tip Number 4
Don't forget to apply through our website! We love seeing candidates who are genuinely interested in joining our team. Plus, it makes it easier for us to keep track of your application and get back to you quickly.
We think you need these skills to ace Senior Statistical Programmer - UK (Remote) Biometrics BELFAST, NORTHERN IRELAND, UNITED KINGDOM
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your mastery in SAS programming and experience with clinical trial databases. We want to see how your skills align with the job description, so don’t be shy about showcasing your relevant experience!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for the Senior Statistical Programmer role. Share specific examples of your past work that demonstrate your expertise in SDTM and ADaM standards.
Showcase Your Problem-Solving Skills: In your application, highlight instances where you've tackled complex problems in statistical programming. We love candidates who can think critically and come up with innovative solutions, so don’t hold back!
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 at StudySmarter!
How to prepare for a job interview at MMS Holdings Inc
✨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 SAS Macros, as this will show your mastery of the tools required for the role.
✨Understand the SDLC
Familiarise yourself with the System Development Life Cycle (SDLC) as it relates to programming deliverables. Be prepared to explain how you've applied this framework in past projects, highlighting your ability to lead study or small programming project teams.
✨Get Acquainted with E-Submission Standards
Review the E-Submission Standards, Guidelines, and Regulations, particularly focusing on SDTM and ADaM standards. You might be asked to write specifications during the interview, so having examples ready will demonstrate your advanced knowledge and experience.
✨Showcase Your Communication Skills
Since good communication is key in this role, think of instances where you've effectively collaborated with others to solve problems. Prepare to discuss how you’ve communicated complex statistical concepts to non-technical stakeholders, as this will highlight your ability to work well in a team.
