Associate Director, CMC Regulatory Affairs - Foster, CA - Gilead Sciences, Inc.

The Regulatory Affairs Coordinator ensures the operational continuity of CAMICO by managing all corporate registrations, insurance licensing and regulatory filings. · High school diploma; 2+ years of administrative or coordinator experience. · ...

+This is an opportunity to work with the Policy and Regulatory Affairs State Team supporting the deployment of the Zoox robotaxi. The intern will have a valuable project on state-level autonomous vehicle policy research and analysis. · +Tackle a substantive project on state-level ...

The Director of Regulatory Affairs will provide regulatory leadership to clinical development programs in oncology. · ...

The Director of Regulatory Affairs is accountable for the delivery of regulatory strategy for designated programs. · ...

+We are seeking a highly motivated Manager who is passionate in the field of cell therapy development for oncology and autoimmune patients. · ...

As a Gilead intern you will contribute to high-impact meaningful projects that will not only further advance our company's mission but will allow you to gain real world experience at one of the most innovative organizations in the world. · ...

We are seeking a Director of Regulatory Affairs to provide regulatory leadership to clinical development programs in oncology. · Degree in biological or life sciences, pharmacy, medicine or related fields. · Direct experience with immuno-oncology drug development and checkpoint i ...

The Global Head of Regulatory Affairs for Companion Diagnostics will define and lead the end-to-end global regulatory diagnostic strategy for the company's portfolio.We are seeking a highly experienced professional to join our team as Global Head of Regulatory Affairs CDx. This r ...

Job summary · The Manager of Regulatory Affairs will provide project teams with regulatory advice, manage and coordinate various Regulatory Affairs activities within and between departments, and obtain and maintain National Health Authority approvals for investigational products. ...

The Senior Associate, Regulatory Affairs reports to a Senior Director, Regulatory Affairs and will support the senior Regulatory team members. · ...

The Associate Director of Regulatory Affairs provides strategic input and management oversight of regulatory labeling activities for multiple products across the Virology therapeutic area.Regulatory Affairs Labeling is a core function within Gilead's Global Regulatory Affairs org ...

The Associate Director, Regulatory Affairs will be responsible for developing and implementing regulatory strategies for development programs to secure and maintain market access in NA for product(s) in line with business objectives. · ...

The Associate Director, Regulatory Affairs will be responsible for developing implementing and advising North America NA regulatory strategies for development programs to secure and maintain market access in NA for product(s) in line with business objectives · 8+ years of experi ...

The Senior Director, Global Regulatory Affairs will play a significant role in providing regulatory strategic leadership on multiple clinical development programs associated with rare diseases in assigned Therapeutic Area (TA). This role will represent the regulatory function and ...

The Senior Director, Global Regulatory Affairs will play a significant role in providing regulatory strategic leadership on multiple clinical development programs associated with rare diseases in assigned Therapeutic Area (TA). This role will represent the regulatory function and ...

The Senior Associate, Regulatory Affairs reports to a Senior Director, Regulatory Affairs and will support the senior Regulatory team members. · We are seeking a highly motivated and enthusiastic individual to continue their growth in regulatory affairs by supporting the implemen ...

The Senior Manager of Regulatory Affairs will provide project teams with regulatory advice and manage various Regulatory Affairs activities within and between departments. · ...

As Principal Regulatory Affairs Specialist at Pulmonx you will drive full spectrum of regulatory activities from initial market authorization through post-market compliance for our US and international device portfolio. · ...

The Senior Manager of Regulatory Affairs will provide project teams with regulatory advice and manage various activities within and between departments. The position may also undertake regulatory intelligence and research. · Manage planning, preparation, coordination, and submiss ...

We are driven by the unique and multi-faceted needs of the PWS community. We value collaboration, integrity, and respect. We are proud to work alongside health care professionals (HCPs) and community members we serve. · We all share the most important goal of bringing solutions t ...

We are seeking a highly motivated and enthusiastic individual to continue their growth in regulatory affairs by supporting the implementation of regulatory strategies for Soleno's development programs from early phase through commercialization. · Prepare routine submissions to he ...