• Coordinator Clinical Research I-Research Oncology…

    MetroHealth (Cleveland, OH)


     

    Biweekly Hours:** **80.00

     

    Shift:** **8a-4:30p

     

    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:

    Plans for, delivers, documents, and observes the progress of subjects enrolled in uncomplicated research studies in accordance with study protocols. These may include observational or interventional trials. Upholds the mission, vision, values, and customer service standards of The MetroHealth System.

    Qualifications:

    Required:

    High School graduate or passage of a high school equivalency exam.

    One-year administrative support or program coordination experience.

    Current Basic Life Support (BLS) certification from the American Heart Association (AHA) or obtains within 90 days of hire.

    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.

    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.

    Administrative support experience in a medical or clinical research setting.

    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.