Over 2 years of clinical research experience and over 3 years in the pharmaceutical industry overall. Extensive knowledge of regulatory documents, contract and budget negotiation, operations management and oversight, study startup, maintenance and closeout activities. Skilled in using Clinical Trial Management Systems (CTMS), e-TMF, Shared Investigator Platform (SIP), EDC, Salesforce and more. Leadership experience includes people management, site management, mentoring and training, creation and initiation on multiple projects and initiatives, leading Maintenance and Closeout Subject Matter Expert (SME) team, and leading regulatory document and submission review team. Clinical trial work covers the following therapeutic areas: Infectious Disease & Vaccine, Respiratory, Women's Health, Cardiology
Advanced Clinical Research Associate Certification (ACRAC) https://app.ccrps.org/certificates/w4whsuhg6p#.YejHyZyF6ho.linkedin