Location: Grayslake, IL
Your Project Coordinator skills are needed just about anywhere. But is it where you want to go? Imagine working for one of the nation’s most respected companies. Making a strategic contribution. Receiving the rewards and recognition you deserve. Whether you are pursuing a contract or permanent placement, Klinexa knows how and where to get you where you want to go.
Are you interested? The ideal Clinical Research Associate candidate will possess the following experience:
Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions. Responsible for writing basic study protocols, monitoring or overseeing monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRFs from study sites, processing CRFs including data cleanup and classification of data, and completion of study summary.
3-5 years of clinical monitoring with experience in the cardiology area or a research coordinator having study experience with patients coming into the emergency department in hospitals or medical centers would also be preferable. Must have Bachelor’s in Scientific area to be considered.