The MetroHealth System (Cleveland, OH)
Coordinator Clinical Research I-Research Oncology Trials
The MetroHealth System (Cleveland, OH), Cleveland, Ohio, us, 44101
Coordinator Clinical Research I-Research Oncology Trials
Apply now for the Coordinator Clinical Research I-Research Oncology Trials role at The MetroHealth System (Cleveland, OH).
Location METROHEALTH MEDICAL CENTER (Cleveland, OH)
Schedule Biweekly Hours: 80.00 Shift: 8-4:30p
About the MetroHealth System 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. 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 equivalent
One year of administrative support or program coordination experience
Current Basic Life Support (BLS) certification from the American Heart Association (AHA) or obtain within 90 days of hire
Proficiency in PC use, 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
Qualifications – 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.
Seniority Level Entry level
Employment Type Full‑time
Job Function
Research, Analyst, and Information Technology
Hospitals and Health Care
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Location METROHEALTH MEDICAL CENTER (Cleveland, OH)
Schedule Biweekly Hours: 80.00 Shift: 8-4:30p
About the MetroHealth System 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. 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 equivalent
One year of administrative support or program coordination experience
Current Basic Life Support (BLS) certification from the American Heart Association (AHA) or obtain within 90 days of hire
Proficiency in PC use, 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
Qualifications – 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.
Seniority Level Entry level
Employment Type Full‑time
Job Function
Research, Analyst, and Information Technology
Hospitals and Health Care
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