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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, and a supportive 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: Opportunity for career growth and to lead process improvement initiatives.
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 City of London 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 City of London
✨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 valuable personal connections can be in landing that dream job.
✨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 boost your confidence.
✨Tip Number 3
Showcase your projects! Create a portfolio of your work, especially any relevant programming or statistical analysis you've done. This gives potential employers a tangible sense of your capabilities.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace Principal or Senior Statistical Programmer - Remote, Office or Hybrid - UK in City of London
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 tools and methodologies you've used, as this will help us see your expertise in action.
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 directly from us. Plus, it’s super easy!
How to prepare for a job interview at Veramed
✨Know Your Stuff
Make sure you brush up on your SAS and R skills before the interview. Be ready to discuss specific projects where you've used these tools, as well as any challenges you faced and how you overcame them.
✨Understand the Clinical Trial Landscape
Familiarise yourself with the clinical drug development process and relevant disease areas. This knowledge will help you answer questions more effectively and show that you're genuinely interested in the role and the company.
✨Showcase Your Leadership Skills
If you're applying for a Principal or Senior role, be prepared to discuss your experience in leading teams or projects. Share examples of how you've managed cross-functional teams or improved processes in previous roles.
✨Ask Thoughtful Questions
Prepare some insightful questions about the company's approach to data management and programming. This not only shows your interest but also helps you gauge if the company culture aligns with your values.
