Clinical Nurse Study Coordinator
US-OH-Cincinnati
US Careers
Req #: 12573
Type: Full-Time
|
|
||||||||||
|
|||||||||||
Overview: Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Responsibilities: * 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. Qualifications: * Bachelor's degree, nursing license (RN); * Clinical experience in acute care setting preferred.
Share this job:
