Experienced clinical trialist in the development of drugs, biologics and diagnostic tests. Extensivebackground in clinical trial management and product evaluation including operational management of large multinational phase III clinical trials which resulted in the regulatory approval of three medications. Experience in medical writing. Authored over a dozen clinical trial reports, other trial related documents such as trial protocols, informed consents, monitoring manuals, drug use patent applications, publications and presentations. Seeking to bring value as a clinical trial operations specialist. Interested in working remotely in a part time or temporary contract situation but willing to consider other opportunities.