Cesar Augusto Perrone Email and Phone Number

Sr. Clinical Research Associate at PPDOct 2012 - Mar 2020Senior Clinical Research Associate: • Perform all duties of a CRA as listed in job title below, serving as the primary contact with individual investigative sites that conduct clinical research for PPD• May track enrollment status reports to ensure study stays on track to meet enrollment goals• May track study-specific status reports to ensure all required information regarding site issues, deviations, and CRF status were kept current by the monitoring team• May serve as mentor/trainer for less experienced CRAs to assist with general and study-specific monitoring issues• May provide direct support to the Clinical Team Manager by assisting with managerial tasks as needed• May perform study-specific training with project team• May develop study-specific monitoring tools and forms for use by monitoring team to assist in efficient review of study data• Perform Serious Adverse Event reconciliation and work with sponsor, study sites and CRAs to resolve discrepancies• Review outstanding data reports and work with CRAs to ensure data collection is met per contractual guidelines• Assist sponsor, study sites, and CRAs with audit preparation/responses and quality issuesNeurology: Multiple SclerosisInfectology: Complicated Urinary Tract InfectionsClinical Research Associate at PPDOct 2010 -- Oct 2012- Monitoring of Clinical Trials according to ICH/GCP guidelines and local regulatory requirements.Clinical Research Associate at Eli LillyMay 2004 — Sep 2010- Monitoring of Clinical Trials according to ICH/GCP guidelines and local regulatory requirements.- In charge of the entire process of a trial (site evaluation, start up training, site initiation visit, monitoring visit, close out, etc) - Experience in trials with different pathologies as oncology, neuroscience, metabolisms.Specialties: * Diabetes (6 studies)* Oncology (5 studies)* Neuroscience (1 study)