Akeem Barry Moore

Clinical Research Associate @IQVIA

Performed site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. Accountable for supporting development of project subject recruitment plan on a per site basis. Worked with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. Provided monitoring visits and site management for a variety of protocols, sites and therapeutic areas. Administered protocol and related study training to assigned sites and established regular lines of communication with sites to manage ongoing project expectations and issues. Evaluated the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalated quality issues as appropriate. Managed 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. Supported start-up phase. Created and maintained 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. Mentored clinical staff including conducting co-monitoring and training visits. Provided assistance with design of study tools, documents and processes including updating monitoring guidelines. Conveyed features and opportunities of study to site. Collaborated and communicated with study team members for project execution support as appropriate. Participated on sponsor calls to discuss trends and site issues.