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- Tasks: Lead statistical programming and analysis for clinical trials, ensuring high-quality outputs.
- Company: Join a leading CRO with a focus on innovation and collaboration.
- Benefits: Competitive salary, flexible hours, generous leave, and comprehensive health benefits.
- Why this job: Make a real impact in clinical research while developing your leadership skills.
- Qualifications: MSc in Statistics or related field, strong SAS and R skills, and experience in clinical trials.
- Other info: Opportunities for mentorship and professional growth in a supportive environment.
The predicted salary is between 36000 - 60000 £ per year.
If you are an experienced statistical programmer who is comfortable moving between statistical leadership and hands-on programming, this role offers the scope and responsibility to match your expertise. We are looking for a Senior Statistical Programmer II to act as a senior technical resource across both statistics and programming functions, with primary alignment to the statistics group. You will play a central role in delivering high-quality clinical trial outputs while supporting, reviewing and strengthening the work of others.
What you will be responsible for:
- You will contribute at a senior level across the full clinical trial reporting lifecycle. This includes:
- Designing and analysing clinical studies, including input into protocols, Statistical Analysis Plans and sample size calculations
- Programming and quality controlling derived datasets and CDISC compliant datasets
- Producing and reviewing Tables, Listings and Figures
- Providing peer review of statistical and programming deliverables
- Ensuring all outputs meet internal SOPs, client requirements and regulatory expectations
You will manage assigned project work independently, communicate clearly with sponsors when required, and flag risks that could affect timelines or data quality. High standards and attention to detail are essential.
Technical expertise required:
- Strong grounding in statistical principles and modelling
- Advanced proficiency in SAS and R for dataset and TLF production
- Excellent knowledge of CDISC standards
- A solid understanding of ICH/GCP guidelines and the regulatory environment
- Experience across multiple study phases and therapeutic areas
This role requires someone who understands not just how to produce outputs, but why they are structured the way they are, and how they will be scrutinised in a regulatory setting.
Leadership and collaboration:
You will line manage assigned team members, providing mentorship, training and performance feedback. Responsibilities include:
- Ongoing supervision and support
- Timesheet approval and resource oversight
- Contribution to annual and interim performance reviews
- Monitoring billability and functional KPIs
You will work closely with Lead Statisticians and Lead Programmers to coordinate delivery and may deputise for a Senior Statistical Programmer III when required. Externally, you will interact directly with clients and contribute to study calls and project meetings.
Requirements:
- MSc in Statistics or a mathematics-based degree with substantial statistical content
- Strong experience as a statistician in a CRO
- Broad experience across clinical trial phases and therapeutic areas
- Strong analytical and problem-solving capability
- Clear written and verbal communication skills, including the ability to explain statistical concepts to non-statisticians
Benefits:
- Competitive Salary (Open to discussion based on experience)
- Home working allowance
- Flexible working hours
- 25 days Annual leave plus bank holidays
- Option to purchase additional days holiday
- Pension with Company matching
- Private medical Scheme with Bupa
- Free standard eye test every two years
- Employee Assistance Program - Available for employee and immediate family
- 5, 10, 15 years of service recognition awards
- Death in service scheme
- Long Term Disability Insurance
- Quanticate offers a variety of different learning development opportunities to help you progress (mentoring, coaching, e-learning, job shadowing)
Senior Statistician I/II employer: Quanticate
Contact Detail:
Quanticate Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Statistician I/II
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on platforms like LinkedIn. We can’t stress enough how personal connections can lead to job opportunities.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to statistical programming. We recommend doing mock interviews with friends or mentors to boost your confidence and refine your answers.
✨Tip Number 3
Showcase your expertise! Bring along examples of your work, such as reports or analyses you've done, to demonstrate your skills during interviews. We want to see how you think and approach problems.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Senior Statistician I/II
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Senior Statistician role. Highlight your statistical programming expertise, especially in SAS and R, and any relevant clinical trial experience.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you're the perfect fit for this position. Share specific examples of your leadership in statistical programming and how you've contributed to successful clinical trials.
Showcase Your Attention to Detail: In your application, emphasise your commitment to high standards and quality control. Mention any experiences where your attention to detail made a significant impact on project outcomes.
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 don’t miss out on any important updates during the process.
How to prepare for a job interview at Quanticate
✨Know Your Stats Inside Out
Make sure you brush up on your statistical principles and modelling techniques. Be ready to discuss how you've applied these in previous roles, especially in clinical trials. This will show that you not only understand the 'how' but also the 'why' behind your work.
✨Show Off Your Programming Skills
Since advanced proficiency in SAS and R is key for this role, prepare to demonstrate your programming skills. You might be asked to solve a problem on the spot or explain your approach to dataset production. Practise coding challenges beforehand to boost your confidence!
✨Understand Regulatory Standards
Familiarise yourself with CDISC standards and ICH/GCP guidelines. Be prepared to discuss how you ensure compliance in your outputs. This knowledge will highlight your attention to detail and understanding of the regulatory environment, which is crucial for the role.
✨Prepare for Leadership Questions
As you'll be managing team members, think about your leadership style and experiences. Be ready to share examples of how you've mentored others or handled project challenges. This will demonstrate your capability to lead and collaborate effectively.