Professor Matt Hammond

BSc, BA, MSc

School of Medicine and Population Health

Director of the Sheffield Clinical Trials Research Unit

Professor of Clinical Trials

Matt Hammond
Profile picture of Matt Hammond
matthew.hammond@sheffield.ac.uk
+44 114 2XX XXXX

Full contact details

Professor Matt Hammond
School of Medicine and Population Health
Barber House
Sheffield
S10 2HQ
Profile

Professor Matt Hammond is Director of the Sheffield Clinical Trials Research Unit (CTRU) within the School of Medicine and Population Health at the University of Sheffield. He is an experienced clinical trials methodologist and senior research leader with over 20 years’ experience working in UKCRC-registered Clinical Trials Units, delivering high-quality multicentre clinical research across a wide range of clinical areas.

Professor Hammond’s expertise spans the full clinical trial lifecycle, including the design, governance, and delivery of CTIMPs, investigational medicinal device studies, and complex intervention trials, from early-phase studies through to large pragmatic randomised controlled trials. Prior to his appointment in Sheffield, he held senior leadership roles at Norwich Clinical Trials Unit, including Deputy Director and Interim Director, where he was responsible for unit strategy, quality systems, regulatory compliance, workforce development, and financial sustainability.

Alongside his operational leadership, Professor Hammond has a strong research interest in trial methodology, innovation, and efficiency. He has led and contributed to several NIHR-funded studies focused on improving trial conduct, including research on electronic consent implementation, automated health record linkage, and screening and recruitment processes. He is currently leading work exploring the operational and financial challenges associated with trial close-out and long-term data archiving, an increasingly important issue for the sustainability of clinical research.

His current methodological interests focus on decentralised and hybrid clinical trial approaches and on improving equality, diversity, and inclusion in research participation. He is a co-applicant on the PRACTICALs (Promoting Accessibility in Clinical Trials) programme, which aims to reduce barriers to trial participation through the development of inclusive, accessible trial processes and training resources.

Professor Hammond plays an active role in the UK clinical trials community. He is a member of the UKCRC Clinical Trials Unit Directors Group and serves as a panel member for the NIHR Research for Patient Benefit (RfPB) programme, contributing to national funding and research strategy. He has extensive experience in research governance and regulatory compliance.

By combining methodological research with senior operational oversight, Professor Hammond’s work aims to support the delivery of efficient, inclusive, and high-integrity clinical trials that better reflect real-world patient populations.

Research interests

Clinical trial methodology, design, and delivery, with a focus on high-quality multicentre randomised controlled trials.

Innovation in clinical trial conduct, including decentralised and hybrid trial models and the use of digital tools to improve efficiency.

Development and evaluation of electronic consent (eConsent).

Screening, recruitment, and retention strategies, including methodological approaches to improving recruitment efficiency and transparency.

Equality, diversity, and inclusion (EDI) in clinical research, with a focus on reducing barriers to participation and improving accessibility of trials.

Governance, regulation, and quality systems in clinical trials.

Sustainability of clinical trials infrastructure, including trial close-out processes, post-funding legacy activities, and long-term data archiving.

Integration of methodological research with Clinical Trials Unit leadership to strengthen applied health research practice and impact.

Publications

Journal articles

Preprints

Professional activities and memberships

Member, UKCRC Clinical Trials Unit Directors Group

Panel Member, NIHR Research for Patient Benefit (RfPB) Programme

Member, Health Research Authority (HRA) Bromley NHS Research Ethics Committee (REC)