Emma Akuffo, BSc, PhD
Director of Study Management

Emma oversees the Study Management, Advanced Research Science and Quality Assurance teams at Richmond Pharmacology.

During her 10 years at Richmond Pharmacology, Emma has worked on over 100 Early Phase Studies ensuring optimal delivery of clinical trial outcomes for our sponsors. This has been achieved through efficient, streamlined processes, the production of high quality documentation and stringent regulatory compliance.

Prior to working at Richmond Pharmacology, Emma worked on various drug development projects within the biotechnology and pharmaceutical industry as well as academia.

Emma is a full member of the British Pharmacological Society and holds a BSc in Biology & Chemistry, PhD in Biochemistry and Postgraduate Certificate in Business Administration.

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Latest news

Clinical trials: how taking the pills can pay those bills.

April 20, 2022
The Guardian references Richmond Pharmacology in feature on reimbursement for clinical trial volunteers
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Clinical trials and the patient perspective

May 6, 2022
Successful recruitment and retention of patients - an essential element to delivering clinical studies on time.
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Events

The Future of Healthcare - March 2022

13:30 – 16:00, 22nd March 2022
Discover the intricacies of assessing abnormal liver functions in clinical trial volunteers and gain insights from the latest drug development trials using RNAi therapeutics.
View event