At a Glance
- Tasks: Lead oncology clinical trials, ensuring quality and compliance while driving innovative research.
- Company: Sheffield Clinical Trials Research Unit, a leader in oncology research.
- Benefits: Competitive salary, flexible work arrangements, and opportunities for professional growth.
- Other info: Join a dynamic team and contribute to high-impact research and teaching.
- Why this job: Make a real impact in cancer research and lead groundbreaking clinical trials.
- Qualifications: Postgraduate in Medical Statistics and extensive oncology trial experience required.
The predicted salary is between 71466 - 75915 € per year.
A non‑clinical position for a Clinical Trial Statistician to serve as academic lead and provide senior oversight and leadership to the Sheffield Clinical Trials Research Unit (CTRU) oncology clinical trials portfolio. The post holder will lead trial design, grant development, submission, and senior‑level study implementation with a specific focus on oncology‑based CTIMPs (Clinical Trials of Investigational Medicinal Products).
Main duties and responsibilities:
- Provide senior oversight and leadership to the CTRU oncology clinical trials portfolio, especially the Yorkshire Cancer Research (YCR) Infrastructure grant, ensuring the project meets its key milestones and deliverables.
- Provide statistical input across the design, conduct, implementation, analysis and reporting of oncology trials within the CTRU portfolio.
- Drive methodological research to advance efficient and patient‑centred trial designs.
- Work collaboratively within a multidisciplinary team including clinicians, statisticians, trial managers and other research professionals.
- Develop a specialist portfolio of oncology research and act as CTRU Lead in collaboration with clinical investigators, designing studies, submitting research applications and securing significant external research income/grant funding.
- Ensure all cancer research studies undertaken under your leadership adhere to randomised controlled trial scientific principles and protocols.
- Oversee quality assurance processes within the CTRU.
- Ensure compliance with all relevant regulatory standards for clinical trials.
- Support preparation for and response to MHRA inspections.
- Lead on the preparation and publication of papers for high‑impact oncology and academic journals.
- Lead on the presentation of findings at international cancer conferences and academic forums.
- Use methodological expertise to undertake research and translational activities that result in demonstrable impact.
- Undertake undergraduate and post‑graduate teaching, supervision and examining within the School of Medicine and Population Health.
- Contribute fully as a researcher, teacher and leader, fulfilling the appropriate requirements of the University's Academic Career Pathway Framework (ACP).
- Make ethical decisions in your role, embedding the University sustainability strategy into your working activities wherever possible.
- Any other duties commensurate with the grade of the post.
Person Specification:
- Postgraduate qualification in Medical Statistics or a closely related discipline.
- Extensive experience in design and analysis of clinical trials within oncology, with a deep understanding of cancer‑specific trial complexities.
- Expertise in complex and innovative trial designs commonly used in oncology (e.g., adaptive designs, master protocols, umbrella/basket trials, dose‑finding Phase I/II designs, and biomarker‑driven trials).
- High and distinctive standing within and outside academia, including major contributions to the field through academic or professional achievement and recognised expertise.
- Sound understanding of the scientific principles of RCTs, including experience with innovative/adaptive trial designs relevant to precision medicine.
- Proven, substantial experience acting as lead statistician on multi‑centre oncology clinical trials.
- Experience working on CTIMPs and thorough knowledge of the Medicines for Human Use (Clinical Trials) Regulations 2004 and ICH Good Clinical Practice (GCP).
- Extensive experience collaborating with senior clinical investigators to design, develop and secure major research grants (e.g., NIHR, CRUK, MRC or major charities).
- A strong track record of high‑quality, peer‑reviewed clinical trial research papers published in high‑impact journals.
- Leadership and mentorship experience supervising junior staff and mentoring early‑career researchers or clinical fellows.
- Excellent skills in maintaining relationships with Chief Investigators, trial funders and Cancer Patient and Public Involvement (PPI) panels.
- Ability to develop creative approaches to complex trial problems (e.g., recruitment barriers in oncology) with an appreciation for long‑term sustainability and strategic aims.
Further Information:
- Grade: Professor up to Band 1.4
- Salary: £71,466 to £75,915 (annual)
- Work arrangement: Full‑time / Part‑time (minimum 0.6 FTE)
- Duration: Permanent
- Line manager: CTRU Director
- Direct reports: Trial Manager, Study Managers, Study Delivery Staff
- Disability confident employer – if you have a disability and meet the essential criteria you will be invited to the next stage of the selection process.
- Closing Date: 02/06/2026
Professor in Medical Statistics and Academic Lead for Clinical Trials in Oncology employer: Diversity Dashboard
As a leading institution in medical research, we offer an exceptional work environment for professionals passionate about oncology and clinical trials. Our collaborative culture fosters innovation and growth, providing ample opportunities for career advancement through mentorship and involvement in high-impact research projects. Located in Sheffield, you will benefit from a vibrant academic community and access to cutting-edge resources, all while contributing to meaningful advancements in cancer treatment and patient care.
StudySmarter Expert Advice🤫
We think this is how you could land Professor in Medical Statistics and Academic Lead for Clinical Trials in Oncology
✨Tip Number 1
Network like a pro! Reach out to your connections in the oncology and clinical trials field. Attend conferences, seminars, or even local meet-ups to get your name out there. You never know who might have a lead on that perfect position!
✨Tip Number 2
Showcase your expertise! Create a personal website or an online portfolio highlighting your research, publications, and any innovative trial designs you've worked on. This is a great way to demonstrate your skills and make a lasting impression.
✨Tip Number 3
Prepare for interviews by brushing up on your knowledge of current trends in oncology and clinical trials. Be ready to discuss your experience with adaptive designs and how you’ve tackled recruitment barriers in past projects. Confidence is key!
✨Tip Number 4
Don’t forget to apply through our website! We’re always looking for talented individuals like you to join our team. Make sure to tailor your application to highlight your leadership experience and your contributions to high-impact research.
We think you need these skills to ace Professor in Medical Statistics and Academic Lead for Clinical Trials in Oncology
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter to highlight your experience in oncology clinical trials. We want to see how your skills align with the specific requirements of the role, so don’t hold back on showcasing your expertise!
Showcase Your Leadership Skills:As this role involves senior oversight, it’s crucial to demonstrate your leadership experience. Share examples of how you've led teams or projects in the past, especially in a clinical trial setting. We love to see candidates who can inspire and guide others!
Highlight Your Research Impact:We’re looking for someone with a strong track record in research. Include details about your published papers and any significant contributions to the field of oncology. This will help us understand the impact you’ve made in your previous roles.
Apply Through Our Website:Don’t forget to submit your application through our website! It’s the best way for us to receive your materials and ensures you’re considered for the position. Plus, it’s super easy to do!
How to prepare for a job interview at Diversity Dashboard
✨Know Your Stats
Brush up on your knowledge of medical statistics, especially in the context of oncology. Be prepared to discuss specific trial designs and methodologies you've worked with, as well as how they apply to the role. This will show your expertise and confidence.
✨Showcase Your Leadership Skills
Since this position involves senior oversight, be ready to share examples of your leadership experience. Talk about how you've successfully led teams in clinical trials, managed projects, and collaborated with multidisciplinary teams. Highlight any mentoring roles you've taken on.
✨Understand the Regulatory Landscape
Familiarise yourself with the Medicines for Human Use (Clinical Trials) Regulations and ICH Good Clinical Practice guidelines. Be prepared to discuss how you ensure compliance in your work and how you handle inspections, as this is crucial for the role.
✨Prepare for Questions on Research Impact
Think about how your research has made a difference in the field of oncology. Be ready to discuss your published papers, grant successes, and any innovative approaches you've developed to tackle complex trial problems. This will demonstrate your commitment to advancing cancer research.
