Clinical Research Associate (CRA) - (Norwood, MA)

The primary point of contact for investigator sites, the CRA ensures the clinical trial is being conducted according to CFR, ICH guidelines and in accordance with GCP. The successful applicant will efficiently execute monitoring and other clinical trial management activities, including tracking the progress of assigned studies/projects and proactively identifying potential challenges. You will develop appropriate actions to resolve issues and achieve target objectives, performing investigator site pre-study site qualification visits including collection of site regulatory documents. A self-motivated individual able work in a small team environment, the CRA is a highly organized individual who can multi-task and adjust direction based on changing project/corporate priorities. You must be flexible and willing to travel.