Clinical Research Coordinator - Part Time

Position Overview We are seeking a highly motivated and detail-oriented Clinical Research Coordinator (CRC) to join our team. The CRC will be responsible for the day-to-day coordination and execution of clinical trials, ensuring compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP). This is an excellent opportunity for someone who thrives in a startup environment and is eager to grow with an organization. Key Responsibilities Coordinate and manage clinical trials from start-up through close-out Screen, recruit, and consent study participants Schedule and conduct study visits per protocol Collect, process, and ship laboratory specimens Accurately document study data in source documents and electronic data capture (EDC) systems Ensure compliance with FDA regulations, ICH-GCP guidelines, and study protocols Maintain regulatory binders and essential documents Communicate with sponsors, CROs, and study monitors Prepare for and participate in monitoring visits, audits, and inspections Track study timelines, enrollment, and patient follow-up Report adverse events and protocol deviations appropriately

Qualifications Required:

Bachelor's degree in health sciences, biology, or related field (or equivalent experience) 1+ years of clinical research experience (or strong clinical background willing to train) Knowledge of GCP and FDA regulations Strong organizational and multitasking skills Excellent communication and interpersonal skills Ability to work independently in a fast-paced environment

Preferred:

Experience in cardiology Experience with EDC systems Phlebotomy and/or clinical skills ACRP or SOCRA certification (or willingness to obtain) What We Offer Competitive salary based on experience Opportunity for career growth Direct exposure to sponsors and leadership Flexible and collaborative work culture