Director, Office of Regulatory Affairs

The American Health Quality Association

Bethesda, MD
Posted Date: 7 days ago

…clinical research. Applicants must have documented expertise and experience in FDA regulatory affairs and review; preparation and processing of IND applications

Vice President of Regulatory Affairs


Salt Lake City, UT
Posted Date: 9 days ago

…can have an impact on the lives of people around the world. The Vice President, Regulatory Affairs will be a member of the Vascular Access Devices (VAD) Business

Regulatory Affairs Specialist

Centura Health

Centennial, CO
Posted Date: 13 days ago

…meet the needs of the clinic may be required. Position Summary The Specialist, Regulatory Affairs will be responsible for regulatory compliance including

Vice President of Regulatory Affairs


Salt Lake City, UT
Posted Date: 11 days ago

Vice President of Regulatory Affairs Posted Date 9 hours ago(7/5/2018 5:27 PM) Industry / Category Medical Device/ Regulatory Affairs Job ID 2018-11724

Director, Regulatory Affairs - Device

Vital Therapies, Inc.

San Diego, CA
Posted Date: 1 days ago

The Director of Regulatory Affairs – Device will identify, review, and anticipate emerging regulatory device issues. The Director will perform a gap analysis

Director, Development Regulatory Affairs

Adamas Pharmaceuticals

Emeryville, CA
Posted Date: 30 days ago

The Director, Development Regulatory Affairs ensures that regulatory expertise is provided for all investigational drug development programs to enable

Senior Director, Clinical Regulatory Affairs

Myovant Sciences Ltd.

Brisbane, CA
Posted Date: 16 days ago

The Senior Director of Regulatory Affairs will provide leadership on global regulatory activities for Myovant. Responsibility includes nonclinical, clinical

Regulatory Affairs Clinical Manager

Bisco Inc

Schaumburg, IL
Posted Date: 2 days ago

Job Description Regulatory Affairs Clinical Manager BISCO has a full time opportunity for a Regulatory Affairs Clinical Manager We are seeking an

TBI Research Coordinator

Chenega Corporation

Bethesda, MD
Posted Date: 27 days ago

…to DVBIC clinical investigations. * Communicates with research participants, staff, regulatory affairs and data management groups, laboratory and clinical

Clinical Trials Monitor - NIH

Kelly Services

Rockville, MD
Posted Date: 6 days ago

…of domestic and international settings. + Provide advice on clinical research operations, regulatory affairs , GCP, or other related clinical research issues such

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