Kamilah Johnson

About Kamilah Johnson

I am a Site Management Associate with a background in clinical research, supporting study…

Experience

1. Clinical Trial Site Management Associate

   PSI CRO

   Jul 2025 — Present · Durham, NC, US

   Ensures exchange of information and documentation with sites and vendors.Ensures order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies. Ensures regulatory and ethics committee submissions and notifications. Coordinates preparation for and follow-up on site, TMF and systems audits and inspections. Reviews and coordinates site-specific query resolution. Supports the organization of internal team meetings including preparation of agendas and minutes. Maintains study specific and corporate tracking systems. Serves as the primary sites contact point for vendors, study supplies, and access management.Ensures communication between the sites and off-site facilities.Prepares, distributes, and updates Investigator Site Files (ISF) and ISF checklists. Provides Monitors with ISF documents to be filed in the ISF prior to each monitoring visit. Tracks vendor-related supplies (lab kits, ECG electrodes, CDs for scans, etc.) on a site level. Assists the Monitors in their prompt completion of all subject event and siteevent information in CTMS.Assists the Monitors in their meeting deadlines for site visits, visit reports and visit letter dates information recording in CTMS. Tracks the resolution status of site issues and action items in CTMS.Ensures proper safety information flow with investigative sites.

Education

• North Carolina State University

  Master of Arts in Teaching, Elementary Education and Teaching

• North Carolina Central University

  Bachelor of Arts - BA, Psychology