Senior Clinical Trials Associate
CurrentPrepared required information for various meetings.Led internal and external meetings. Created and shipped binders (Investigator Site Files), Informed Consent Forms and other documentation to sites. Supported distribution of clinical and ancillary supplies to the sites. Reviewing monthly financial metrics and using funds per budget.Maintained study portals and distribution lists.Managed user access to study systems.Filing documents to the TMF.Managed project training matrix, team list and CTMS.Created monthly newsletters.Mass communication to sites.Coordinated and led the team of Clinical Trials Associates on large clinical projects. Identifying risks.Interviewing, coaching, training and development of new employees.