Senior Clinical Affairs Specialist (Memphis, AR)

Senior Clinical Affairs Specialist

SUMMARY This position is responsible for FDA regulated and postmarket clinical studies associated with assigned products. This includes assuring that all clinical research documentation and regulatory submissions comply with applicable US and International government regulations guidelines and company standards. The position is also responsible for managing the investigator sites in assigned studies to ensure they are in compliance with the agreement the protocol the IRB applicable US and International regulations and sponsor instructions. The incumbent possesses an extensive knowledge of all aspects of clinical research gained through experience and is able to perform the essential duties and responsibilities with little...read moreApply NowCompany