Clinical Research Associate - CRA (Level Depending on Experience)

Job description

About CTI CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com What You’ll Do: - Serve as main CTI contact for assigned study sites - Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP - Assist with or oversee study start-up activities, including feasibility, pre-study activities and site selection - Collect, review and track essential/regulatory documents - Participate in and complete all general and study specific training as required - Participate in investigator, client and...