Crissy Ford

About Crissy Ford

Experienced Senior Clinical Research Associate with a demonstrated history of working in…

Experience

1. Sr Cra 3

   IQVIA

   May 2021 — Present

   Perform site selection, initiation, interim and close-out monitoring visits in accordance with contracted scope of work and good clinical practice. • Provide monitoring visits and site management for a variety of phase 1, 2 and 3 protocols and sites in pediatric and adult oncology. • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Project Manager (PM), Clinical Lead (CL) and/or Site & Resource Manager (SRM). • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. • Liaise between Investigators, study coordinators, vendors, IQVIA clinical team and sponsor teams to ensure the smooth running of the protocol and to minimize protocol deviations. • Mentor new CRAs by accompanying new CRAs on their first monitoring visits as well as allowing new CRAs to perform job shadowing Focused on Oncology and Hematology clinical trials.