Research Coordinator III - Center for Cardiovascular Genomics and Data Science

At Cleveland Clinic Health System, we believe in a better future for healthcare. And each of us is responsible for honoring our commitment to excellence, pushing the boundaries and transforming the patient experience, every day. We all have the power to help, heal and change lives — beginning with our own. That’s the power of the Cleveland Clinic Health System team, and The Power of Every One. Job Title Research Coordinator III - Center for Cardiovascular Genomics and Data Science Location Cleveland Facility Cleveland Clinic Main Campus Department HVTI Research and Registries-Heart Vascular & Thoracic Institute Job Code T99497 Shift Days Schedule 8:00am-5:00pm Job Summary Job Details Join Cleveland Clinic’s Main Campus where research and surgery are advanced, technology is leading-edge, patient care is world class and caregivers are family. Here, you will work alongside a passionate and dedicated team, receive endless support and appreciation, and build a rewarding career with one of the most respected healthcare organizations in the world. Groundbreaking discoveries happen every day at Cleveland Clinic, where every team member contributes to advancing patient care, research, and education. As Research Coordinator III, you will oversee complex research programs within HVTI’s Center for Cardiovascular Genomics & Data Science, taking on substantial independent responsibility for coordinating research protocols, developing protocols and research infrastructure, ensuring research data quality, and collaborating with investigators, research personnel, external partners, and research administration. A caregiver in this position works Monday through Friday from 8:00 a.m. – 5:00 p.m. A caregiver who excels in this role will: Demonstrate exceptional coordination and compliance of the implementation and conduct of human subject research projects. Assist with research study design and protocol development as applicable. Independently direct large, complex, multi-center clinical research protocols/programs and coordinate the implementation and conduct of research projects, ensuring adherence to research protocol. Report Serious Adverse Events and/or safety as they occur and complete Food and Drug Administration (FDA) and sponsor forms in accordance with GCP guidelines. Communicate with sponsors, monitors and research personnel to ensure all aspects of study compliance. Serve as a liaison between investigators, research personnel, outside study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions. Collaborate with primary investigators, sponsors and research caregivers to plan, conduct and evaluate project protocols, including research subject recruitment. Monitor and report project status. Complete regulatory documents, data capture and monitoring plans. Complete and oversee protocol related activities. As delegated, attain and maintain clinical competencies for unlicensed caregivers, such as phlebotomy, vital signs, ECG, POC testing and other testing as required. Oversee and monitor research data to maintain quality. Develop and maintain knowledge of research protocols to coordinate the comprehensive and compliant execution of assigned protocols. Assist with the preparation for audits and response to audits. Develop or assist in the development and maintenance of research tools, such as spreadsheets, questionnaires and/or brochures. Maintain study personnel certification records (License, CV, CITI). Conduct and document the informed consent process. Assist the PI with research study design and development of research protocol. Submit the study to appropriate agencies in support of the research programs and assist with annual and other reporting requirements. Contribute to or assist with research project budget development. Minimum qualifications for the ideal future caregiver include: High School Diploma or GED and five years of experience as a Research Coordinator II or performing the role of a Research Coordinator II OR Bachelor’s Degree in a healthcare or science-related field and three years of experience Proficient with a variety of computer-based skills (word processing, Outlook, Excel, spreadsheets, databases and presentation software) Preferred qualifications for the ideal future caregiver include: Associate’s or Bachelor’s Degree in a healthcare or science-related field Physical Requirements: Ability to perform work in a stationary position for extended periods Ability to operate a computer and other office equipment Ability to communicate and exchange accurate information In some locations, ability to move up to 25 pounds Personal Protective Equipment: Follows standard precautions using personal protective equipment as required. The policy of Cleveland Clinic Health System and its system hospitals (Cleveland Clinic Health System) is to provide equal opportunity to all of our caregivers and applicants for employment in our drug free environment. All offers of employment are followed by testing for controlled substances. Cleveland Clinic Health System administers an influenza prevention program. You will be required to comply with this program, which will include obtaining an influenza vaccination on an annual basis or obtaining an approved exemption. Decisions concerning employment, transfers and promotions are made upon the basis of the best qualified candidate without regard to color, race, religion, national origin, age, sex, sexual orientation, marital status, ancestry, status as a disabled or Vietnam era veteran or any other characteristic protected by law. Information provided on this application may be shared with any Cleveland Clinic Health System facility. If applying for a Florida position, please see the following website for more information on the background screening requirements required by the Agency of Health Care Administration: Please review the Equal Employment Opportunity poster . Cleveland Clinic is pleased to be an equal employment opportunity employer.