<p>We are seeking a full-time, experienced Clinical Research Coordinator (CRC). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.</p> <p>Responsibilities:</p> <ul> <li>Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management. </li><li>Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation </li><li>Schedule all patient research visits and procedures consistent with protocol requirements </li><li>Conduct patient visits as outlined within each study protocol </li><li>Dispense study medication, collect vital signs and perform ECGs </li><li>Perform blood draws, process and ship specimens per study protocol and IATA regulations </li><li>Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms. </li><li>Act as point of contact for study participants </li><li>Adhere to Research SOPs, Good Clinical Practices, and the study protocols </li><li>Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager and PI throughout course of the study </li><li>Ensure all safety data is reviewed by the PI in a timely manner </li><li>Maintain inventory of study equipment and supplies onsite at all times </li><li>Participate actively in communication of status and results to management </li><li>Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol </li><li>Schedule and prepare for monitor visits </li><li>Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations </li><li>Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance </li><li>Complete and maintain case report forms per FDA guidelines, and review them against the patient's medical record for completeness and accuracy </li></ul> <p>Iterative Health Expectations</p> <p>All employees are expected to:</p> <ul> <li>Perform quality work within deadlines with or without direct supervision </li><li>Interact professionally with other employees, customers and suppliers </li><li>Work effectively as a team contributor on all assignments </li><li>Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations </li></ul> <p>Qualifications</p> <ul> <li>Medical Assistant, LPN, Associates or Bachelor's degree in a clinical or scientific-related discipline preferred </li><li>Minimum 1-2 years of clinical research experience </li><li>Able to execute on research tasks with guidance from more experienced staff, PIs, and management </li><li>Strong written and verbal communication skils </li><li>Ability to read, interpret, and apply clinic policies and research protocols </li><li>Ability to use standard office software </li><li>Must be able to lift up to 25 pounds </li></ul>