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 workplace culture that fosters 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 High Wycombe employer: Veramed
Veramed is an exceptional employer that prioritises a warm and friendly working environment, fostering both personal and professional growth. With a supportive management approach and a commitment to employee development, we offer unique opportunities for career advancement in the dynamic field of clinical trials. Our remote or hybrid working options, combined with a focus on collaboration and integrity, make Veramed a standout choice for skilled Statistical Programmers looking to make a meaningful impact.
StudySmarter Expert Advice🤫
We think this is how you could land Principal or Senior Statistical Programmer - Remote or Hybrid - UK in High Wycombe
✨Network Like a Pro
Get out there and connect with people in the industry! Attend conferences, webinars, or local meetups. We can’t stress enough how important it is to build relationships; you never know who might have the inside scoop on job openings.
✨Show Off Your Skills
When you get the chance to chat with potential employers, don’t hold back! Share your experience with SAS and any R programming skills you have. We want to see your passion and expertise shine through in conversations.
✨Prepare for Interviews
Do your homework before interviews! Familiarise yourself with Veramed’s projects and values. We recommend practising common interview questions and preparing examples of how you've tackled challenges in previous roles.
✨Apply Through Our Website
Don’t forget to apply directly through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take that extra step to engage with us directly.
We think you need these skills to ace Principal or Senior Statistical Programmer - Remote or Hybrid - UK in High Wycombe
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the role of Principal or Senior Statistical Programmer. Highlight your SAS experience and any R skills you have, as well as your understanding of clinical trials. We want to see how your background fits with what we do!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about statistical programming and how your experience aligns with our values at Veramed. Show us your personality and enthusiasm for the role!
Showcase Your Technical Skills:In your application, be sure to highlight your technical skills, especially in SAS and R. Mention specific projects where you've applied these skills, and don't forget to include any experience with clinical trial documents and data management!
Apply Through Our Website:We encourage you to apply through our website for a smooth application process. It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity. We can’t wait to hear from you!
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.
