4 years of experience as a Clinical Research Data Coordinator with Virginia Oncology Associates7 months of experience as a Vascular Clinical Research Coordinator with Sentara Health Research Center. Responsibilities include studying specific procedures and regulations to be carried out according to protocol. Assisting with recruitment, screening, enrolling, and scheduling patients in research trials according to study-specific protocol. Completing all electronic Case Report Forms (eCRFs) promptly while ensuring the accuracy of data entry. Maintaining subject and regulatory e-binders. Resolving patient queries promptly and communicate with study sponsor. Promptly reporting Adverse Events and Serious Adverse Events according to protocol and IRB regulations. Communicating with local IRB to ensure adherence to using the most recent IRB approved consents and protocol. Organizing and attending Site Initiation Visits, participating in Coordinator calls, and traveling to Investigator Meetings. Collect and communicate necessary study-specific information to ensure compliance and open communication across the various affected department areas. Obtain patient vital signs, perform phlebotomy, process specimen collections, and upload images into Core lab portal. Follow up with scheduled meetings with Principal Investigator’s for appropriate signatures. Interact and assist with monitor visits. Ensure accuracy and completion of Device Accountability Logs and Drug Accountability Logs.