Westat is an employee-owned corporation providing research services to agencies of the U.S. Government, as well as businesses, foundations, and state and local governments. Westat's research, technical, and administrative staff of more than 2,000 is located at our headquarters in Rockville, Maryland, near Washington, DC.
Westat is seeking a qualified Regulatory Affairs (RA) Research Associate to support clinical trials regulatory compliance for a contract research organization (CRO).
Responsibilities include, but are not limited to: writing and compiling regulatory documents for submissions to health authorities; performing regulatory review and approval of site regulatory documents prior to trial initiation; interacting with site study coordinators and investigators, developing a conducting trainings, independently researching and writing on assigned topics; providing regulatory guidance in cross-functional teams; performing regulatory review of trial related documents, processing of serious adverse event reports; creating, updating, and tracking study-specific regulatory files; providing support to the Regulatory Affairs Director; ensuring that all work activity is performed in accordance with established procedures and regulatory requirements.
Westat offers competitive benefits with ESOP, 401k, Health, Dental, paid vacation, sick and holiday leave, professional development as well as other benefits.
Any offer of employment may be contingent upon receipt of acceptable results from a post-offer background screening, if required for the position, based on the specific position which may include, for example, identity verification, employment history, or criminal records history.
Westat is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, sex, age, national origin, veteran status, disability, or any other classification protected by Federal, state, or local law.