Experienced Clinical Research Associates / Monitors Needed for Clinical Trials

Kelly Scientific Resources is seeking experienced Clinical Research Associates for opportunities throughout the US. Common therapeutic areas include: Cardiovascular, Diabetes, Hypertension, Oncology, Infectious Diseases, Medical Device, and CNS.These positions would be responsible for monitoring activities at various clinical study sites to assure adherence to regulatory guidelines (GCP, ICH), SOPs, and study protocols. Review regulatory documents as required and prepare site visit reports. Must be able to manage multiple projects and to work both independently and in a team environment. May participate in the study development and start-up process including reviewing protocols, designing and/or reviewing CRFs, preparing Informed Consent forms, developing study documents, organizing and presenting at investigator meetings, working with management on monitoring strategy, and/or developing project-specific CRA training. These positions require a bachelor's degree (scientific or nursing discipline) with a minimum of three years of field experience as a Clinical Research Associate monitoring multiple sites, performing the tasks described above. Positions include both company- and home-based opportunities and may be contract, contract-to-hire, or direct-hire in nature. Lead positions may also be available. For 60 years, Kelly Services has provided outstanding employment opportunities, including temporary, temp-to-hire, and direct placement, to the most talented individuals in the marketplace. Learn more about company