Global Regulatory Affairs Lead, Clinical Programs
$170k - $210kAllogene Therapeutics
Allogene Therapeutics is seeking an Associate Director of Regulatory Affairs to oversee global regulatory strategy and submissions. This hybrid role requires expertise in interactions with regulatory agencies like the FDA and knowledge of cell therapy regulations. Candidates should have a bachelor’s degree and 7+ years of regulatory experience. The position offers a competitive salary range of $170,000 - $210,000 annually, based in South San Francisco. #J-18808-Ljbffr
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- ...and Early Development (gRED) The gRED Global Clinical Trial Leader (CTL) is accountable for... ...leadership of the Sr. CTL. These complex programs focus on the rapid development of new... ...of GCP/ICH requirements, international regulatory guidelines, and the end to end drug development...SuggestedLocal areaMonday to FridayFlexible hours
- ...Position Title : Global Clinical Trial Leader (CTL) Work Location : South San Francisco, CA... ...leadership of the Sr. CTL. These complex programs focus on the rapid development of new... ...of GCP/ICH requirements, international regulatory guidelines, and the end to end drug development...SuggestedLocal areaRemote workMonday to FridayFlexible hours
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- ...Title: Global Clinical Trial Leader Location: South San Francisco, CA... ...the Sr. CTL. These complex programs focus on the rapid development... ...requirements, international regulatory guidelines, and the end to... ...we connect top talent with leading organizations through trusted...SuggestedLocal areaRemote workMonday to FridayFlexible hours
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...experienced Associate Director, Clinical Regulatory in South San Francisco. The role focuses on leading regulatory strategy for development programs in neurodegenerative... ...interactions with global Health Authorities and... ...significant regulatory affairs experience, and strong...- ...Description Job Description Global Clinical Trial Leader (CTL) Location:... ...early development programs with the potential to transform... ...Key Responsibilities Lead operational execution of global... ...ICH guidelines, international regulatory requirements, and the drug development...Contract workLocal areaRemote workWorldwide
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...Position: Global Clinical Trial Leader (GCTL) Location: 1 DNA Way, South San Francisco, CA 94080 Duration: 12-Month Contract (Potential... ...Working knowledge of GCP, ICH guidelines, international regulatory requirements, and the end-to-end drug development process....Weekly payContract workMonday to Friday3 days per week$245k - $318k
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...hard for a mission that matters at a company where you matter. Your Impact You will serve as the strategic manager of Axon's global travel program, owning our most impactful vendor relationships and ensuring travelers have access to the best possible travel benefits and...Contract workWork at officeRemote work- Monograph is seeking an experienced Program Manager to lead large-scale programs that drive operational excellence across teams. The role involves building collaborative relationships with stakeholders and managing complex projects in a fast-paced environment. Ideal candidates...Work at officeRemote work
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