At a Glance
- Tasks: Lead and support programming efforts for clinical studies in a dynamic environment.
- Company: Join ClinChoice, a global CRO focused on quality and professional development.
- Benefits: Enjoy remote work, competitive salary, and opportunities for career growth.
- Other info: Be part of a diverse team committed to inclusivity and continuous training.
- Why this job: Make a real impact in the healthcare industry while working with innovative technologies.
- Qualifications: Strong SAS programming skills and experience in CVRM studies required.
The predicted salary is between 60000 - 80000 £ per year.
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds. ClinChoice is searching for a Principal Statistical Programmer Consultant to join one of our clients in the CVRM team. ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.
Main Job Tasks and Responsibilities:
- The Principal Statistical Programmer Consultant is a delivery-focused role who works under the leadership, oversight, and direction of a Programming team leader to lead and/or support aspects of the programming effort to deliver technical programming and information components of a project. This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasks.
Key Requirements:
- Strong SAS programming experience within the pharmaceutical/CRO industry
- Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies
- Experience in generating and validating SDTM, ADaM, and TLFs
- Good understanding of CDISC standards and clinical trial processes
- Ability to work independently and manage multiple priorities in a fast-paced environment
- Experience supporting regulatory submissions is preferred
- Strong communication and stakeholder management skills
Responsibilities:
- Develop, validate, and maintain SAS programs for clinical study data analysis and reporting
- Create datasets, tables, listings, and figures according to study requirements
- Collaborate with Biostatistics, Data Management, and Clinical teams
- Ensure programming deliverables meet quality standards and project timelines
- Participate in study planning, review specifications, and support submission activities
Education and Experience:
- Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5 years of clinical programming (CDISC) experience; Master’s degree in CS, statistics or related disciplines with 6 years of clinical programming (CDISC) experience.
- Need to have Respiratory/Immunology TA experience.
- Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology.
The Application Process:
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for a phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
About ClinChoice:
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos:
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
Principal Statistical Programmer/Analyst Consultant Remote at UK (CVRM- Cardiovascular , Renal & Metabolism)-(Outside IR35) employer: ClinChoice
ClinChoice is an exceptional employer that offers the unique opportunity to work directly with a single sponsor while benefiting from the stability and career growth potential of a global CRO. With a strong emphasis on professional development, a supportive work culture, and a commitment to diversity and inclusivity, employees are empowered to thrive in their roles. The company's focus on quality and continuous training ensures that team members are equipped with the skills needed to excel in the fast-paced clinical research environment.
StudySmarter Expert Advice🤫
We think this is how you could land Principal Statistical Programmer/Analyst Consultant Remote at UK (CVRM- Cardiovascular , Renal & Metabolism)-(Outside IR35)
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work at CROs or in CVRM. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your SAS programming skills and understanding CDISC standards. We want you to feel confident discussing your experience and how it aligns with the role.
✨Tip Number 3
Showcase your communication skills! During interviews, highlight examples of how you've successfully collaborated with teams or managed stakeholders. This is key for client-facing roles like this one.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Principal Statistical Programmer/Analyst Consultant Remote at UK (CVRM- Cardiovascular , Renal & Metabolism)-(Outside IR35)
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Principal Statistical Programmer role. Highlight your SAS programming experience and any relevant CVRM studies you've worked on. We want to see how your skills match what we're looking for!
Showcase Your Experience:Don’t just list your past jobs; explain what you did in each role, especially around generating SDTM, ADaM, and TLFs. We love seeing concrete examples of your work that demonstrate your technical skills and industry knowledge.
Be Clear and Concise:Keep your application clear and to the point. Use bullet points where possible to make it easy for us to read. We appreciate a well-structured application that gets straight to the important stuff!
Apply Through Our Website:We encourage you to apply through our website for the best chance of getting noticed. It’s the easiest way for us to track your application and ensure it reaches the right people. Don’t miss out!
How to prepare for a job interview at ClinChoice
✨Know Your SAS Inside Out
Make sure you brush up on your SAS programming skills, especially in the context of CVRM studies. Be ready to discuss specific projects where you've developed, validated, or maintained SAS programs, and how you ensured they met quality standards.
✨Understand CDISC Standards
Familiarise yourself with CDISC standards and clinical trial processes. Prepare to explain how you've applied these standards in your previous roles, particularly in generating SDTM, ADaM, and TLFs.
✨Showcase Your Communication Skills
Since this role involves client interaction, practice articulating your thoughts clearly and confidently. Think of examples where you've successfully managed stakeholder relationships or collaborated with cross-functional teams.
✨Prepare for Regulatory Discussions
Brush up on your knowledge of regulatory submissions and ICH guidelines. Be prepared to discuss your experience in supporting regulatory activities and how you ensure compliance in your programming tasks.
