Call:
+44 (0) 1865 784074
Oxford Vacmedix UK Limited:
Oxford, UK, OX4 4GA
Email:
enquiries@oxfordvacmedix.com
- Seeking Series B investment for next phase of clinical trials
Call:
+44 (0) 1865 784074
Oxford Vacmedix UK Limited:
Oxford, UK, OX4 4GA
Email:
enquiries@oxfordvacmedix.com
Dr Thomas Morris
Chief Medical Officer
Dr Thomas Morris is a physician who has worked in drug development for over 20 years, specialising in oncology. He has worked for Medeval Ltd (University of Manchester) and AstraZeneca, overseeing several global drug development programmes.
He has a BSc in Physiology from the University of Wales, medical degrees from the University of Wales College of Medicine, and his Master of Laws degree from Cardiff Law School. He is a Fellow and Board member of The Faculty of Pharmaceutical Medicine, a former chair of its Ethical Issues committee and a member of its Professional Standards Committee.
Mark Thomas (FGK Clinicology Ltd)
Head of Clinical Operations
Mark has a BSc. (Hons) in Medical Microbiology from the University of Surrey and over 25 years industry experience across pharmaceutical and clinical research organisations (CROs).
He was previously a founding director/Board member of a medium size CRO and also held senior clinical operations roles at Swiss and US Pharma companies. Mark has extensive experience leading global oncology clinical studies.
Debra Nevin PhD (Amethyst Pharma Ltd)
Manufacturing
Debra is a freelance CMC Consultant who specialises in Biologics manufacturing development for clinical trial material from early stage through to late stage development. Experienced in CDMO outsourcing and manufacturing project management, with over 25 years’ experience in CMC technical and Quality support.
Dr Thomas Morris
Chief Medical Officer
Dr Thomas Morris is a physician who has worked in drug development for over 20 years, specialising in oncology. He has worked for Medeval Ltd (University of Manchester) and AstraZeneca, overseeing several global drug development programmes.
He has a BSc in Physiology from the University of Wales, medical degrees from the University of Wales College of Medicine, and his Master of Laws degree from Cardiff Law School. He is a Fellow and Board member of The Faculty of Pharmaceutical Medicine, a former chair of its Ethical Issues committee and a member of its Professional Standards Committee.
Mark Thomas (FGK Clinicology Ltd)
Head of Clinical Operations
Mark has a BSc. (Hons) in Medical Microbiology from the University of Surrey and over 25 years industry experience across pharmaceutical and clinical research organisations (CROs).
He was previously a founding director/Board member of a medium size CRO and also held senior clinical operations roles at Swiss and US Pharma companies. Mark has extensive experience leading global oncology clinical studies.
Dr Thomas Morris
Chief Medical Officer
Dr Thomas Morris is a physician who has worked in drug development for over 20 years, specialising in oncology. He has worked for Medeval Ltd (University of Manchester) and AstraZeneca, overseeing several global drug development programmes.
He has a BSc in Physiology from the University of Wales, medical degrees from the University of Wales College of Medicine, and his Master of Laws degree from Cardiff Law School. He is a Fellow and Board member of The Faculty of Pharmaceutical Medicine, a former chair of its Ethical Issues committee and a member of its Professional Standards Committee.
Mark Thomas (FGK Clinicology Ltd)
Head of Clinical Operations
Mark has a BSc. (Hons) in Medical Microbiology from the University of Surrey and over 25 years industry experience across pharmaceutical and clinical research organisations (CROs).
He was previously a founding director/Board member of a medium size CRO and also held senior clinical operations roles at Swiss and US Pharma companies. Mark has extensive experience leading global oncology clinical studies.
Debra Nevin PhD (Amethyst Pharma Ltd)
Manufacturing
Debra is a freelance CMC Consultant who specialises in Biologics manufacturing development for clinical trial material from early stage through to late stage development. Experienced in CDMO outsourcing and manufacturing project management, with over 25 years’ experience in CMC technical and Quality support.
Laura Lugo (DLRC Ltd)
Regulatory
Laura Lugo is a senior Regulatory Consultant at DLRC, a specialist consultancy providing high quality regulatory services to a wide range of clients. Laura has a over 15 years experience in the pharmaceutical industry, with over 10 years in regulatory affairs. She specialises in supporting global regulatory activities, particularly in the develoment stage, including clinical trial applications, paediatric investigation plans and orphan drug designations. Prior to joining DLRC, she has worked with GSK, Cellzone and PPD.
Debra Nevin PhD (Amethyst Pharma Ltd)
Manufacturing
Debra is a freelance CMC Consultant who specialises in Biologics manufacturing development for clinical trial material from early stage through to late stage development. Experienced in CDMO outsourcing and manufacturing project management, with over 25 years’ experience in CMC technical and Quality support.
Laura Lugo (DLRC Ltd)
Regulatory
Laura Lugo is a senior Regulatory Consultant at DLRC, a specialist consultancy providing high quality regulatory services to a wide range of clients. Laura has a over 15 years experience in the pharmaceutical industry, with over 10 years in regulatory affairs. She specialises in supporting global regulatory activities, particularly in the develoment stage, including clinical trial applications, paediatric investigation plans and orphan drug designations. Prior to joining DLRC, she has worked with GSK, Cellzone and PPD.
Lisa Mynheer
Technical Support Manager
Lisa has been providing sector specific business support to start-ups, SME’s and their leaders in life sciences for over 20 years. She specialises in helping businesses to exploit their innovations and grow. Lisa provides project management and technical support to projects and the CEO. She holds a BSc. in Combined Science from the University of Leicester and a Post Graduate Certificate in Coaching and Facilitation in Organisations from the University of Chester. She was previously Operations Director at Oxford Bio-Innovation Ltd, and Senior Consultant and Business Coach at Oxford Innovation Ltd, as well as running her own Coaching and Innovation advisory business.
Laura Lugo (DLRC Ltd)
Regulatory
Laura Lugo is a senior Regulatory Consultant at DLRC, a specialist consultancy providing high quality regulatory services to a wide range of clients. Laura has a over 15 years experience in the pharmaceutical industry, with over 10 years in regulatory affairs. She specialises in supporting global regulatory activities, particularly in the develoment stage, including clinical trial applications, paediatric investigation plans and orphan drug designations. Prior to joining DLRC, she has worked with GSK, Cellzone and PPD.
Lisa Mynheer
Technical Support Manager
Lisa has been providing sector specific business support to start-ups, SME’s and their leaders in life sciences for over 20 years. She specialises in helping businesses to exploit their innovations and grow. Lisa provides project management and technical support to projects and the CEO. She holds a BSc. in Combined Science from the University of Leicester and a Post Graduate Certificate in Coaching and Facilitation in Organisations from the University of Chester. She was previously Operations Director at Oxford Bio-Innovation Ltd, and Senior Consultant and Business Coach at Oxford Innovation Ltd, as well as running her own Coaching and Innovation advisory business.
Contact Us
If you have any questions or want to get in touch, please contact our team.
(c) 2025 Oxford Vacmedix UK Limited | Company Registration: 07994205
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