Clinical Trial Specialist
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My career in Clinical Research started in 1998. I have performed duties such as: CTA, PV Specialist, Clinical Relations Specialist and Practice Manager. My passion is to work in Clinical Research
I have a vast knowledge of ICH/GCP and have a strong ethics code. My Pharmacovigilance journey has made me gain a great deal, whilst networking in IPASA. Learning regulatory reporting responsibilities of other countries. My CTA and SSC experience taught me a good work ethic and working very well in a team capacity.
I have a N3 Business and Office certificate. During my 24 years in the Pharmaceutical industry, I was invited and attended many Investigators Meetings for different Therapeutic Areas and won a Project Excellence award for positive initiatives.
