Paul Carter

Paul has 30+ years’ experience in both CRO and pharmaceutical industries (AstraZeneca) as a study director/study monitor on a range of studies, including all delivery routes and species but specialising as an inhalation toxicologist.  For the last 10 years at AstraZeneca, Paul led the global strategic implementation of preclinical outsourcing of inhalation toxicology studies.  A recognised international expert in the field of inhalation toxicology/aerosol science, Paul has been an active committee member of the Association of Inhalation Toxicologists since 1987. Paul is a versatile toxicologist within the pharmaceutical arena and has all round knowledge of all processes involved in drug research and development.

Abigail Walker

MSc

Abigail Walker is a scientific writer with experience in toxicology, neuroscience, neurobiology and nutrition, having graduated from the University of Glasgow with a BSc and MSc in Neuroscience.  A keen communicator, she enjoys expanding her knowledge base, drawing out the key points in complex scientific subjects and working collaboratively in teams.

Joanne Wilson

Joanne has more than 20 years of experience as a DMPK scientist and project manager gained at AstraZeneca.  In this role, she led cross-functional teams to drive the optimal and efficient development of novel drugs. Joanne has worked across all therapy areas with a special expertise in oncology.  Joanne brings a blend of scientific expertise and project management skills to optimise drug discovery and development processes.

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Stacey Owen

Stacey is an experienced customer facing professional programme manager with extensive experience in nurturing and establishing long-term relationships to ensure optimal delivery.  She is an excellent communicator with the experience needed to manage complex projects with rapidly changing and competing priorities.  A true customer advocate, Stacey brings calmness and clarity to provide the best service possible, eliciting and listening to feedback to improve outcomes.

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Dr Sarah Pass

Sarah is an experienced drug metabolism and pharmacokinetics (DMPK) consultant, having worked for almost 30 years in the pharmaceutical and CRO industries, providing a wide range of expertise to academia, biotechnology and pharmaceutical companies.  A collaborative project leader, Sarah has broad experience ranging from lead identification though to end of Phase II clinical development.  Sarah is passionate about making a difference to patients’ lives and delivering decision-making data to accelerate new drugs through the R&D pipeline.

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Dr Craig Thomas

PhD

Craig has extensive expertise in toxicology, discovery research, competitive intelligence and due diligence spanning more than three decades. He began his career at the Marion Merrell Dow research institute where he worked in Cardiovascular and CNS discovery before joining Eli Lilly in 1996 where he focused on increasing the efficiency and predictability of early phase safety assessment. Building on this, he spent two years leading cross-functional due diligence then progressed to lead strategic competitive intelligence for neuroscience, including conducting drug target assessments.  Craig is passionate about the critical role toxicology plays in delivering innovative molecules with optimal risk-benefit profiles to address major unmet medical needs.

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Henry Bushell

Henry has a keen interest in economics and decided to acquire some business experience, joining ApconiX straight from sixth form college.  Playing an active role within business development, Henry hopes to gain an understanding of how businesses become and remain successful before going on to study economics at university.  An active mind and a willingness to take on new projects, Henry is well suited to the very busy, very demanding workload of a growing company.

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William Humfrey

MSc

Will studied for an integrated master’s degree in biomedical science at the University of Sheffield where he gained understanding of human health, disease processes and developed both practical and written skills. Particularly enjoying literature searches, critical reviews, data analysis and report writing, Will is keen to learn new skills as part of the target safety assessment team.

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Michelle Blissett

MSc

With almost 20 years devoted to preclinical toxicology, Michelle has developed an excellent ability to conduct extensive literature searches, interrogating, analysing and interpreting data and has contributed to regulatory and scientific reports and produced numerous literature reviews.  As a Senior Toxicologist, Michelle has experience of clinical chemistry, haematology, cytogenetics and conducting preclinical studies for clients globally.  A collaborative and articulate communicator, Michelle has an aptitude for conveying complex scientific data in an accurate and concise manner.

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Scott Hackford

MSc

Scott has over 12 years’ experience at a UK CRO where he was Senior Toxicologist, Study Director, and manager of a team of study directors.  As Senior Toxicologist, Scott advised clients on drug safety programs across multiple therapy areas and therapeutic modalities. This work included the design, conduct and reporting of nonclinical safety studies to support regulatory submissions.  Scott has experience with agrochemical and chemical industry clients and the relevant regulatory guidelines including REACH.  Collaborating with clients to obtain the best outcomes, Scott is easy to approach, always working to enable projects are completed in a timely manner.

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