Coord Clinical Research I

3 weeks ago

Cleveland, United States Metro Health Full time

**Location:** **METROHEALTH MEDICAL CENTER** **Biweekly Hours:** **80.00** **Shift:** **8-4:30** **The MetroHealth System is redefining health care by going beyond medical treatment to improve the foundations of community health and well-being: affordable housing, a cleaner environment, economic opportunity and access to fresh food, convenient transportation, legal help and other services. The system strives to become as good at preventing disease as it is at treating it. Founded in 1837, Cuyahoga County’s safety-net health system operates four hospitals, four emergency departments and more than 20 health centers.** **Summary:** **The Northeast Ohio Regional Spinal Cord Injury (SCI) System is seeking a people-oriented human research coordinator. Major duties include interacting with people living with SCI to enroll as research participants, conducting multiple study-specific interviews, extracting data from electronic medical records, and coordinating study visits that may be in-person or virtual. Major skills needed include the ability to connect with people of all backgrounds, superb communication, meticulous attention to detail, and the ability to work with a diverse team in a fast-paced environment. This position is in-person at the MetroHealth Center for Rehabilitation Research at the Old Brooklyn Campus.** Qualifications: Required: High School graduate or passage of a high school equivalency exam. One-year administrative support experience in a medical or clinical research setting. Demonstrated high level of proficiency in the use of a PC, including Word and Excel. Excellent interpersonal, written, and verbal communication skills. Strong analytical skills. High level of organizational skills. Ability to assess and reprioritize quickly to meet deadlines in a fast-paced environment. Ability to work independently. Required to learn various hospital systems. Ability to interact effectively with a wide range of cultural, ethnic, racial, and socioeconomic backgrounds. Preferred: Associate’s Degree. Two years’ experience working with Federal Regulations relating to human subject research. Institutional Review Board (IRB) experience. Certified clinical research coordinator (CCRC). Physical Demands: May need to move around intermittently during the day, including sitting, standing, stooping, bending, and ambulating. May need to remain still for extended periods, including sitting and standing. Ability to communicate in face-to-face, phone, email, and other communications. Ability to read job related documents. Ability to use computer.

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