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Doctrine Analyst, Quantico, VA
Posted 6 days ago
to relieve suffering for people with great needs, but few options. We are dedicated to discovering and developing life changing treatments for patients with under addressed neurological, endocrine and psychiatric disorders. The company's diverse portfolio includes FDA approved treatments for tardive dyskinesia, Parkinson's disease, endometriosis and uterine fibroids , as
Posted 17 days ago
Office of The Chief Financial Officer
- Washington, DC / Maryland, MD / Tysons Corner, VA
LIHTC,General Counsel, tax credit, affordable housing, economic development, community development
Posted 27 days ago
Sempra Infrastructure seeks an outstanding regulatory attorney with deep subject matter expertise in development and management of power projects and energy commodity trading to join the Legal Department in Houston or San Diego. This attorney will be responsible for a portfolio of complex and time sensitive legal matters, with a focus on the regulation of electric transac
Posted 1 month ago
Intel Analyst, Quantico, VA
Posted 6 days ago
Senior Government Biller Collector Facility Prime Healthcare Management Inc Location US CA Ontario ID 2024 161134 Category Admin Position Type Full Time Shift Days Job Type Non Exempt Overview Prime Healthcare is an award winning health system headquartered in Ontario, California. Prime Healthcare operates 45 hospitals and has more than 300 outpatient locations in 14 stat
Posted 21 days ago
of Position Responsibilities The Senior Proposal Development Officer has responsibility for preparing proposal submissions from faculty, staff, and students of the University, including determining if project proposals are consistent with the academic and research policies of the University. Advises faculty, staff, and students on the development of project proposals, the
Posted 10 days ago
Prepares /oversees the preparation of various regulatory submissions including Pre Submissions, 510(k) submissions, CLIA Waiver Applications, Dual 510(k)/Waiver by Applications, technical files, and license applications. Monitors new and changing regulations and guidance and disseminates information to stakeholders. Identifies regulatory trends and conducts key regulatory
Posted 30 days ago
Benefits Start Day 1 for Full Time Colleagues No Waiting Period! For more information about our benefits, see below! We are proud to be a member of the Rentokil family of companies, the global leader in Pest Control and other services across more than 90 countries. We pride ourselves on being a trusted partner to many of the world's leading brands and serve consumer and b
Posted 23 days ago
Site Name USA Pennsylvania Upper Providence, GSK House, Switzerland Zug, USA Massachusetts Waltham, USA North Carolina Durham Posted Date May 16 2024 Purpose Ensure the development of appropriate Precision Medicine and Digital Health regulatory strategy(s) and their execution for assigned precision medicine and digital health asset(s) supporting across the GSK therapeutic
Posted 22 days ago
Parexel's Strategic CGMP Compliance team is known for our unparalleled breadth and depth of expertise globally. Parexel CGMP Compliance offers services which create and maximize product value for clients throughout the product lifecycle, leveraging our unique fusion of scientific, regulatory, and business expertise. We are the pre eminent regulatory and GxP (Good Clinical
Posted 18 days ago
JMSEL/JNEM Planner position in Suffolk, VA
Posted 10 days ago
Develop solutions to improve processes for global regulatory submissions. Identify, implement, support validation and manage software tools for organizing regulatory files, registration tracking and documentation for submissions Manage Regulatory tools/database and new enhancements. Interact with global regulatory leaders and peers to share and manage department metrics a
Posted 1 month ago
Liaison Officer from Joint Forces to the US Navy- Suffolk, VA
Posted 12 days ago
Reviews and interprets regulations/guidance documents to develop regulatory strategy to support Transfusion Medicine project teams in terms of regulatory submission pathway, IND & CMC strategies, submission requirements, timing and risks. Interact with US FDA and acts as a liason with Corporate International RA and/or country RA to define submission content, expedite pend
Posted 1 month ago
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