Clinical Research Coord III- College of Nursing

Bachelor's degree in an appropriate area and five years of relevant experience; or an equivalent combination of education and experience. ACRP or SOCRA certification

• Oversees implementation of research projects, including regulatory compliance, screening participants, ensuring appropriate scheduling and follow-up for research participants, and supervising staff and volunteers involved in the research projects. Act as liaison for research subject, investigator, IRB, sponsor, and healthcare professionals. Develop advertisement materials. Develop and revise informed consent document to ensure compliance with IRB. Perform specimen collection, storage, processing, and shipment in accordance with study protocol. Runs subjects in experimental protocols; involves obtaining informed consent, administering questionnaires, completing brain imaging, and conducting sensory testing protocols (including experimental pain testing).
• Manages data; includes developing online data management systems, maintaining subject charts and scanning paper forms and upload them to the central database. Ensure that all paper and computer files are maintained in a confidential manner. Participates in the development and conduct of study billing plans. Manage study finances including sponsor invoicing & resolving study subject billing issues.
• Maintains effective written and verbal communication with PIs and other lab members and participates actively in lab meetings.
• Maintains the inventory and schedule of the laboratory. Includes ordering supplies; tracking equipment, computers, and phones; and maintaining copies of questionnaires for use in the study. Schedules staff meetings and tracking work schedules. Schedules participant appointments in research studies.
• Trains other research and volunteer research assistants in data collection and data management; ensures their compliance with IRB and privacy policies.

• Previous clinical research experience and/or pain research experience and demonstrate experience in clinical research coordination
• Strong problem-solving, communication, and organizational skills
• Ability to work independently and collaboratively in a fast-paced environment
• ACRP or SOCRA certification