At a Glance
- Tasks: Lead oncology clinical trials, ensuring high-quality design and implementation.
- Company: Sheffield Clinical Trials Research Unit, a leader in cancer research.
- Benefits: Competitive salary, flexible work arrangements, and opportunities for professional growth.
- Other info: Join a dynamic team and contribute to groundbreaking cancer research.
- Why this job: Make a real impact in oncology research and advance your academic career.
- 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 in Sheffield employer: Diversity Dashboard
As a leading institution in medical research, the University offers an exceptional work environment for professionals in the field of oncology. With a strong emphasis on collaboration and innovation, employees benefit from extensive opportunities for professional growth, mentorship, and involvement in groundbreaking research that directly impacts patient care. The supportive culture fosters a commitment to excellence, ensuring that staff are equipped to thrive in their roles while contributing to significant advancements in clinical trials.
StudySmarter Expert Advice🤫
We think this is how you could land Professor in Medical Statistics and Academic Lead for Clinical Trials in Oncology in Sheffield
✨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 and learn about potential job openings.
✨Tip Number 2
Showcase your expertise! Create a personal website or an online portfolio that highlights your research, publications, and any innovative trial designs you've worked on. This is a great way to stand out and demonstrate your skills.
✨Tip Number 3
Prepare for interviews by brushing up on your knowledge of current trends in oncology clinical trials. Be ready to discuss your experience with adaptive designs and how you can contribute to the CTRU's mission.
✨Tip Number 4
Don't forget to apply through our website! We want to see your application and hear about your passion for advancing oncology research. Make sure to highlight your leadership experience and collaborative spirit in your application.
We think you need these skills to ace Professor in Medical Statistics and Academic Lead for Clinical Trials in Oncology in Sheffield
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 Contributions:Don’t forget to mention any significant research papers or contributions you’ve made to the field. We’re looking for someone with a strong track record, so include details about your publications and presentations at conferences to make your application stand out.
Apply Through Our Website:We encourage you to submit your application through our website for a smoother process. It’s the best way to ensure your application gets the attention it deserves, and we can’t wait to see what you bring to the table!
How to prepare for a job interview at Diversity Dashboard
✨Know Your Stats Inside Out
As a Clinical Trial Statistician, you need to be well-versed in statistical methods and oncology trial designs. Brush up on adaptive designs, master protocols, and the complexities of cancer trials. Be ready to discuss how your expertise can drive methodological research and improve patient-centred trial designs.
✨Showcase Your Leadership Skills
This role requires senior oversight and leadership, so prepare examples of your past experiences leading teams or projects. Highlight your ability to collaborate with multidisciplinary teams and your success in securing research grants. Demonstrating your leadership style will show that you're the right fit for this academic lead position.
✨Familiarise Yourself with Regulatory Standards
Understanding the Medicines for Human Use (Clinical Trials) Regulations and ICH Good Clinical Practice is crucial. Be prepared to discuss how you've ensured compliance in previous roles and how you would approach quality assurance processes within the CTRU. This knowledge will set you apart as a candidate who takes regulatory standards seriously.
✨Prepare for Academic Contributions
Since you'll be expected to publish papers and present findings, think about your past publications and conference presentations. Be ready to discuss your research impact and how you plan to contribute to high-impact journals. This will demonstrate your commitment to advancing the field of oncology through your work.
