EU Regulatory Compliance Specialist — Drug​/Device Trials

A leading pharmaceutical firm is seeking a Regulatory Compliance Specialist to support a Quality Management System initiative focused on drug/device combination products. The role involves ensuring compliance with EU clinical trial regulations and streamlining internal processes. Ideal candidates will have strong experience in regulatory compliance and a proven track record in a pharmaceutical setting. This is a full-time, remote position with a preference for East Coast candidates.
We are looking to fill the EU Regulatory Compliance Specialist — Drug/Device Trials position at Medasource in NJ, United States. The EU Regulatory Compliance Specialist — Drug/Device Trials role at Medasource is now open for applications in NJ, United States. Join us at Medasource as our next EU Regulatory Compliance Specialist — Drug/Device Trials in NJ, United States. We are currently recruiting a EU Regulatory Compliance Specialist — Drug/Device Trials for our team in NJ, United States.