Medpace, Inc.
Location
Cincinnati, Ohio
The Clinical Nurse Study Coordinator is responsible for the accurate administration of medications, monitoring of adverse events, and performing clinical procedures according to study protocols. They also collaborate with project managers and investigators to ensure operational flow and data integrity.
Candidates must hold a Bachelor's degree and a valid nursing license (RN). Previous clinical experience in an acute care setting is preferred.
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Study Coordinator to join our Clinical Pharmacology Unit team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
May assist in interviewing, evaluating, and scheduling prospective study subjects according to protocol criteria; Responsible for accurate and safe administration of medications according to protocols; Responsible for assessing subjects for adverse events and ensuring they are documented; Perform and/or schedule procedures (e.g. vital signs, intravenous insertions, venipunctures, laboratory tests, ECGs, etc.); Work closely with Project Managers on operational matters (i.e. study execution planning, operational flow); Interacts with study Monitors and resolving data queries, confirming eligible subjects, and interacting with the Investigator for medical matters.
Bachelor's degree, nursing license (RN); Clinical experience in acute care setting preferred.
Why Medpace?
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