- Kelly Services (Sunnyvale, CA)
- Kelly(R) Science & Clinical is seeking a Regulatory Affairs Process Specialist for a one-year contract opportunity with a leading molecular diagnostics ... Remote US (Pacific and Central Time preferred **)** **Position Title:** Regulatory Affairs Process Specialist **Position Type:** One-year contract… more
- Amazon (Sunnyvale, CA)
- …Frames. Working as part of the Medical Devices Operational Compliance Team (MD-OCC), the Sr. Regulatory Affairs Specialist will be working to build best in ... product post-marketing approval requirements. * Supports the product release process . * Acts as an SME for internal and...dollar businesses and reporting to senior leadership - . Regulatory Affairs Certification (RAPS) - . Drug… more
- Kelly Services (Sunnyvale, CA)
- **Senior Regulatory Affairs Specialist I** **Overview:** The Senior Regulatory Affairs Specialist I, NPD is responsible for evaluating and ... R&D, and Clinical Affairs , as part of client's global change control process . The position ensures regulatory compliance of product labeling and offers… more
- Stanford University (Stanford, CA)
- Regulatory Specialist **School of Medicine, Stanford, California, United States** Research Post Date Nov 12, 2024 Requisition # 105179 TheBlood and Marrow ... for patients worldwide. BMT-CT is seeking a Clinical Trials Regulatory II Specialist to support a very...in a dynamic research setting. + Strong knowledge of regulatory affairs , including FDA regulations, IRB review… more
- Stanford University (Stanford, CA)
- … regulatory requirements, or experience working with an IRB. . Knowledge of regulatory affairs , including FDA regulations, IRB review and approval process ... Clinical Trials Regulatory and Quality Specialist **School of...external policies. . Manage and oversee new study initiation process , including educating study staff and sponsors, resolving issues… more
- Stanford University (Stanford, CA)
- … regulatory requirements, or experience working with an IRB. + Knowledge of regulatory affairs , including FDA regulations, IRB review and approval process ... Clinical Events Committee Specialist I **School of Medicine, Stanford, California, United...compile research protocol documents and all materials required for regulatory submissions in compliance with University and external policies.… more