At a Glance
- Tasks: Provide programming support for clinical trials using SAS and R, ensuring data quality and compliance.
- Company: Veramed, a unique CRO focused on collaboration and innovation in clinical trials.
- Benefits: Remote or hybrid work, competitive salary, training, and a supportive environment.
- Other info: Enjoy a warm, friendly workplace with opportunities for personal and professional growth.
- Why this job: Join a caring team and make a real impact in the world of clinical research.
- Qualifications: 6+ years in statistical programming with SAS; R skills are a bonus.
The predicted salary is between 60000 - 80000 £ per year.
Clinical trials are high stakes, demanding high standards. Veramed sets this standard by bringing together the sharpest minds in data management, biostatistics and programming, with cutting-edge technology and proven processes. Our globally connected, caring team delivers quality, precision and collaboration, earning trust through consistency and integrity. From rapid-fire project work to long-term partnerships, Veramed brings the right minds to every challenge.
We have an exciting opportunity for a Principal or Senior level Statistical Programmer skilled in SAS to join us on a permanent basis in the UK. If you have any R Programming skills this would be a bonus. We can offer home and/or office working, training and support and a competitive package.
The purpose of the role is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. The Senior or Principal Programmer may also perform a supervisory role (e.g. line management and/or project management).
Key Responsibilities- Previous experience with SAS and some R experience/knowledge.
- Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs.
- Author, review and approve study TFL shells and dataset specifications.
- Author, validate and document SAS programs for datasets, TFLs and macros, applying good programming practice.
- Identify data issues and outliers.
- Complete, review and approve CDISC Validation tool reports.
- Identify data and standards issues and resolve or escalate as appropriate.
- Awareness of emerging standards and associated impact to ongoing and future planned trials.
- Maintain proficiency in SAS and awareness of developments.
- Maintain study master file documents and any other documents that are required to be audit ready.
- Lead internal and client study, project and cross functional team meetings effectively.
- Present study updates internally and at client meetings.
- Share scientific, technical and practical knowledge within the team and with colleagues.
- Perform work in full compliance with applicable internal and client policies, procedures, processes and training.
- Build effective collaborative working relationships with internal and client team members.
- Ensure learnings are shared across projects or studies.
- Develop and provide internal technical training where appropriate.
- Lead process improvement initiatives.
- BSc, MSc or PhD in numerical discipline (or relevant equivalent industry experience).
- At least 6 years of relevant industry experience.
- Understanding of clinical drug development process, relevant disease areas, endpoints and study designs.
WHAT TO EXPECT: A warm, friendly working environment in which to thrive both personally and professionally. A supportive, open-door management policy that will aid in your development and provide you with the tools to take your career to the next level. A truly unique CRO that's doing something different when it comes to managing staff, projects and building relationships in the industry. The ability to own your role and develop your skills and experience.
Principal or Senior Statistical Programmer - Remote or Hybrid - UK in Milton Keynes employer: Veramed
Veramed is an exceptional employer that fosters a warm and friendly working environment, allowing employees to thrive both personally and professionally. With a strong emphasis on support and development, the company offers flexible working arrangements, comprehensive training, and opportunities for career advancement, making it an ideal place for skilled Statistical Programmers to grow their expertise in a collaborative and innovative setting.
StudySmarter Expert Advice🤫
We think this is how you could land Principal or Senior Statistical Programmer - Remote or Hybrid - UK in Milton Keynes
✨Tip Number 1
Network like a pro! Reach out to professionals in the industry on LinkedIn or at events. We can’t stress enough how important it is to make connections that could lead to job opportunities.
✨Tip Number 2
Prepare for interviews by practising common questions and showcasing your SAS skills. We recommend doing mock interviews with friends or using online resources to boost your confidence.
✨Tip Number 3
Showcase your projects! If you’ve worked on relevant clinical trials or programming tasks, be ready to discuss them in detail. We love seeing real examples of your work and how you tackled challenges.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for talented individuals who are passionate about making a difference in the field.
We think you need these skills to ace Principal or Senior Statistical Programmer - Remote or Hybrid - UK in Milton Keynes
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that match the job description. Highlight your SAS and R programming experience, as well as any relevant clinical trial work. We want to see how you fit into our world!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to tell us why you're passionate about statistical programming and how your background aligns with our values at Veramed. Keep it friendly and professional – we love a good story!
Showcase Your Technical Skills:Don’t just list your technical skills; demonstrate them! If you've authored or validated SAS programs, mention specific projects or outcomes. We’re keen on seeing how you’ve applied your knowledge in real-world scenarios.
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 us you’re proactive – a quality we admire!
How to prepare for a job interview at Veramed
✨Know Your SAS Inside Out
Make sure you brush up on your SAS skills before the interview. Be prepared to discuss specific projects where you've used SAS, and be ready to demonstrate your understanding of good programming practices. If you have any experience with R, don’t forget to mention that too!
✨Understand Clinical Trials
Familiarise yourself with the clinical trial process and the role of a statistical programmer within it. Be ready to talk about how you’ve contributed to previous trials, including your experience with protocols, SAPs, and CRFs. This will show that you understand the high stakes involved.
✨Showcase Your Leadership Skills
If you're applying for a Principal or Senior role, highlight any supervisory or project management experience you have. Prepare examples of how you've led teams or projects, and how you’ve built collaborative relationships with clients and colleagues.
✨Prepare Questions for Them
Interviews are a two-way street! Think of insightful questions to ask about their processes, team dynamics, and how they support professional development. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
