Clinical research professional
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I have over ten years of experience working in clinical research in monitoring and administrative roles.
I have over ten years of experience working in clinical research for the company that is now known as Fortrea. I have most recently worked as a Clinical Research Associate II, monitoring sites for diabetes medical device trials. I've also spent two years monitoring pharmacies for mostly oncology trials, as well as monitoring hospitals for a trial in hepatology.
I am adept as an unblinded clinical research associate and have worked on over ten trials in this capacity, and successfully closed out multiple sites. Prior to that, I have had roles such as In-house CRAI, Clinical Research Assistant, Senior Clinical Project Administrator and Clinical Project Administrator. I have a strong background in administration for clinical trials, working in both international and national teams across a breadth of therapeutic areas and phases.
I have a wealth of experience in dealing with research documentation and administrative duties, being well versed in handling Investigator Site Files and Trial Master Files. I've been heavily involved in helping with an FDA site inspection and assisted with multiple MHRA inspections as well as internal and sponsor audits.
I have a Psychology degree from the University of Reading for which I received an upper second class.
I attended the International School of Dakar and obtained Advanced Placement Credits which are equivalent to A levels, for the subjects of Psychology, Biology and English Literature. I received an A, A and B respectively.