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 options, 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 Lincoln 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 an attractive 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 Lincoln
✨Tip Number 1
Network like a pro! Reach out to professionals in the industry through LinkedIn or local meetups. 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 skills. We recommend doing mock interviews with friends or using online platforms to boost your confidence.
✨Tip Number 3
Showcase your projects! If you’ve worked on relevant clinical trials or programming tasks, create a portfolio. We love seeing real examples of your work that demonstrate your expertise.
✨Tip Number 4
Apply directly through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re genuinely interested in joining our team at Veramed.
We think you need these skills to ace Principal or Senior Statistical Programmer - Remote or Hybrid - UK in Lincoln
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 expertise and any R programming knowledge you have, as these are key for us at Veramed.
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 concise but impactful!
Showcase Your Experience:When detailing your previous roles, focus on specific projects where you've demonstrated your programming skills and leadership abilities. We love to see examples of how you've tackled challenges in the past.
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 unique team!
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 key documents involved, like protocols and SAPs. Being able to talk knowledgeably about these will show that you understand the high stakes of the role and can contribute effectively from day one.
✨Showcase Your Leadership Skills
If you're applying for a Principal or Senior role, be ready to discuss your experience in leading teams or projects. Think of examples where you've successfully managed a project or mentored a colleague, as this will highlight your ability to take on supervisory responsibilities.
✨Prepare Questions for Them
Interviews are a two-way street! Prepare thoughtful questions about the company culture, team dynamics, and ongoing projects. This not only shows your interest but also helps you gauge if Veramed is the right fit for you.
