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- 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: Flexible working options, competitive salary, training support, and a friendly work environment.
- Why this job: Join a caring team and make a real impact in the world of clinical research.
- Qualifications: BSc, MSc or PhD in a numerical discipline with 6+ years of industry experience.
- Other info: Opportunities for personal and professional growth in a supportive atmosphere.
The predicted salary is between 36000 - 60000 £ 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 & R to join us on a permanent basis in the UK. 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 R.
- 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, Office or Hybrid - UK in West End employer: Veramed
Contact Detail:
Veramed Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal or Senior Statistical Programmer - Remote, Office or Hybrid - UK in West End
✨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 and R skills. We recommend doing mock interviews with friends or using online platforms to get comfortable with the process.
✨Tip Number 3
Showcase your projects! Whether it's through a portfolio or discussing them in interviews, we want to see how you've applied your programming skills in real-world scenarios. It’s all about demonstrating your expertise.
✨Tip Number 4
Don’t forget to apply through our website! We’re always looking for talented individuals like you, and applying directly can sometimes give you an edge. Plus, it shows your enthusiasm for joining our team!
We think you need these skills to ace Principal or Senior Statistical Programmer - Remote, Office or Hybrid - UK in West End
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 experience with SAS and R, and any relevant projects you've worked on. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical trials and how your background makes you a great fit for our team. Keep it friendly and professional – we love a personal touch!
Showcase Your Technical Skills: In your application, don’t forget to showcase your technical skills, especially in programming and data management. Mention specific projects where you’ve used SAS and R, and any challenges you overcame. We appreciate detail and clarity!
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of applications and ensures you get all the updates. Plus, it’s super easy – just follow the prompts and let us know you’re interested!
How to prepare for a job interview at Veramed
✨Know Your SAS and R Inside Out
Make sure you brush up on your SAS and R skills before the interview. Be prepared to discuss specific projects where you've used these tools, and think about any challenges you faced and how you overcame them. This will show that you're not just familiar with the software, but that you can apply it effectively in real-world scenarios.
✨Understand Clinical Trials Thoroughly
Since the role involves working with clinical trial documents, take some time to review the key components like protocols and SAPs. Familiarise yourself with the drug development process and be ready to discuss how your experience aligns with the responsibilities outlined in the job description. This will demonstrate your commitment and understanding of the industry.
✨Prepare for Team Dynamics
Given the emphasis on collaboration and leading meetings, think about examples from your past where you've successfully worked in a team or led a project. Be ready to share how you build relationships and communicate effectively with both internal teams and clients. This will highlight your interpersonal skills, which are crucial for this role.
✨Showcase Your Problem-Solving Skills
The job requires identifying data issues and resolving them. Prepare to discuss specific instances where you've encountered data challenges and how you approached solving them. This could involve technical solutions or process improvements, so think broadly about your experiences and be ready to share them.
