medical devices in both the U.S. and Europe, support of international product registrations and related regulatory affairs... Regulatory Affairs experience in Medical Device regulations. Demonstrated success in taking products through FDA and EU Notified...
Hours of Work : 8am-5pm Days Of Week : M-F Work Shift : Job Description : Your Job: The Regulatory Specialist... will perform expertise in the regulatory component of all clinical research trials to include, but not limited to; Phase II and IV...
Hours of Work : 8am-5pm Days Of Week : M-F Work Shift : Job Description : Your Job: The Regulatory Specialist... will perform expertise in the regulatory component of all clinical research trials to include, but not limited to; Phase II and IV...