Job Description:

Summary: We are seeking a dedicated Clinical Research Coordinator to collaborate with Investigators in the execution of Phase I, II, III, and IV clinical research trials, ensuring adherence to Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols. With a commitment to delivering exceptional patient care, the Clinical Research Coordinator will play a pivotal role in every interaction.Shift: Monday-Friday, 8:00 AM - 5:30 PM (Paid overtime available for weekend, evening, or early morning work as needed)Compensation: Hourly Rate based on experience + comprehensive benefits, PTO, and 401k matchResponsibilities:Obtain informed consent from study participantsExecute study protocol procedures meticulously, maintaining organization and professionalismConduct human specimen lab draws and processing, and handle specimen shipmentsGenerate and complete study source documents and report adverse events using an e-source systemManage study-specific files and maintain adequate suppliesLiaise with Study SponsorCRO for study-specific inquiriesParticipate in site visits, including site initiation and monitoring visits from SponsorsCROsQualifications:Degree in Psychology or related fieldPrevious experience in neurology studies is advantageousPhlebotomy experience preferredIdeally, possess 2+ years of experience as a Clinical Research Coordinator