Oversee the quality assurance of all Good Pharmacovigilance Practice (GVP) activities to ensure that third party vendors remain compliant with and prepared for potential Sponsor & Regulatory Inspections, and ensure that the appropriate processes, systems, and activities are in place and performed to protect the rights, safety and welfare of patients participating in clinical trials.
May telecommute from any location in the US.
Application Instructions:
Apply at https://www.blueprintmedicines.com/careers/ or via email to Careers@blueprintmedicines.com.
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