We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our innovative research team. In this pivotal role, you will be responsible for the successful execution and management of clinical trials, ensuring adherence to study protocols, regulatory guidelines, and Good Clinical Practice (GCP). You will work closely with investigators, study participants, and sponsors, managing all aspects from patient recruitment and consent to data collection and query resolution. This is an exciting opportunity to contribute to cutting-edge medical advancements and make a tangible difference in patient care. Skills: Clinical trial protocol interpretation, Electronic Data Capture (EDC) systems, Informed Consent process, Patient recruitment and retention strategies, Regulatory document management, Drug accountability, Specimen collection and processing, Excellent written and verbal communication, Time management and organization Requirements: Bachelor's degree in a life science, healthcare, or related field, Minimum of 2 years of experience as a Clinical Research Coordinator or equivalent role, Proficient knowledge of FDA regulations, ICH Guidelines, and Good Clinical Practice (GCP), Experience with IRB submissions and continuing reviews, Ability to work independently and collaboratively in a fast-paced environment, Strong problem-solving abilities and attention to detail, Certification (e.g., ACRP, SoCRA) preferred but not required, Current BLS certification