Director, Regulatory Affairs - San Francisco

We are looking for a Regulatory Affairs Consultant to support several ongoing projects at about 10-20 hours per week. This role is remote. · Job Duties · Work closely with Pharmatech and our client's executive leadership team to lead the development of regulatory strategies and o ...

+This isn't your typical regulatory affairs position. You'll be teaching AI systems how to think like a regulatory professional. · ...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The Senior Manager of Regulatory Affairs will provide project teams with regulatory advice and manage various ac ...

This innovative patient-focused commercial-stage biopharmaceutical company based in China and US is seeking a Regulatory Affairs Director who can lead development implementation of regulatory strategy for key oncology asset. · ...

We are seeking a Director of Regulatory Affairs to drive the preparation and execution of global regulatory NDA/MAA filings for late-stage oncology programs. The successful candidate will have a thorough understanding of oncology drug development, US NDA & global filing regulatio ...

· Job Description · Primary Job Functions: Provide administrative support for the activities conducted by the Regulatory Affairs Department. Ensure timely and effective assessments of new regulatory information to determine impact on Illumina products and processes.  · Secondary ...

The Director of Regulatory Affairs is accountable for driving preparation & execution of Regulatory NDA/MAA filings for late-stage oncology programs at RevMed. · ...

The Regulatory Affairs Specialist will support regulatory compliance activities by preparing and executing submissions to FDA and other global regulatory agencies. · ...

Career-defining. Life-changing. · At iRhythm, you'll have the opportunity to grow your skills and your career while impacting the lives of people around the world. iRhythm is shaping a future where everyone, everywhere can access the best possible cardiac health solutions. Every ...

Director, Global Regulatory Affairs (Oncology) · Location: South San Francisco, CA (Hybrid) · Remote: Can be considered · Compensation: $235-270K base + 20% bonus + equity · Target Start: Mid‑April · About the Company · Our client is a global, commercial‑stage biopharmaceutical c ...

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

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. · Define and execute a global companion diagnostic regulatory strategy aligned with the company's precision oncol ...

We're transforming how regulatory documents get written in pharma biotech and medtech through fundamental AI research. · The Role · You'll be teaching AI systems how to think like a regulatory professional evaluating AI-generated content identifying gaps in logic or compliance de ...

We are a non-profit committed to our participants. Dedicated To The Care Of Elders PACE (Program of All-Inclusive Care for the Elderly) was developed to answer the many problems around caring for frail seniors. Seniors, their family members, and caregivers face many issues... · ...

About us: · Braveheart Bio is a Bay Area–based biopharmaceutical company pioneering best-in-class therapies for cardiovascular disease. Our lead program is a next-generation myosin inhibitor, licensed from Hengrui Pharma, being developed to transform the treatment of hypertrophic ...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS p ...

We are a non-profit committed to our participants. Dedicated to The Care of Elders: PACE (Program of All-Inclusive Care for the Elderly) was developed to answer the many problems around caring for frail seniors. The PACE model is centered on the belief that it is better for the w ...

This is a Regulatory Affairs Manager position supporting preparation review submission CMC sections U.S global regulatory filings INDs CTAs amendments BLAs MAAs coordinating internal stakeholders gather technical information ensure accuracy consistency CMC documentation developin ...

Proclinical is seeking a Senior Director Regulatory Affairs for a growing and exciting clinical-stage biotechnology company based in the San Francisco Bay Area California. · In this role you will lead global regulatory strategy and operations across the companys development pipel ...

We are looking for a Sr Manager Regulatory Affairs who will define the regulatory strategy plans and objectives for assigned products compounds indications or projects in Virology. · Doctorate and 2+ years of relevant experience OR Master's and 6+ years of relevant experience OR ...