Global Regulatory Lead, Oncology - Strategy & Submissions
$226k - $270kDormont Manufacturing Co
Immunome, Inc. is seeking a Global Regulatory Lead in Bothell, Washington, to drive the regulatory strategy for its oncology therapies. The role involves leadership of the Global Regulatory Team, developing regulatory strategies, and ensuring compliance throughout product development. Applicants should have a Bachelor’s degree in a scientific discipline and over 10 years of experience in regulatory affairs. A history of successful regulatory submissions and a focus on oncology is strongly preferred. The pay range is $226,000—$270,000 annually. #J-18808-Ljbffr Dormont Manufacturing Co
$226k - $270k
...a clinical-stage targeted oncology company committed to developing... ....Position OverviewAs the Global Regulatory Lead at Immunome, you will be... ...global regulatory strategies for our therapeutic portfolio... ...local regulations for global submissions.Stakeholder CommunicationCommunicate...RegulatoryLocal areaFlexible hours- Immunome, Inc. in Bothell, WA, is seeking a Global Regulatory Lead to shape and execute regulatory strategies across its oncology portfolio. You will collaborate with cross‑functional teams to navigate global submissions (INDs, BLAs, NDAs), manage health authority interactions...Regulatory
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$288.03k - $353.64k
...informed drug development across its oncology portfolio. The ideal candidate will have... ...PK, dose optimization, and regulatory submissions. This highly visible role involves leadership... ...in designing pharmacometrics strategies, collaborating with various departments...Regulatory- ...an experienced leader to steer the global inline breast cancer portfolio strategy, translating market insights into... ...priorities and ensuring alignment with oncology and enterprise goals. You will... ...major congresses and forums, and lead portfolio planning. #J-18808-Ljbffr...
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$177.4k - $238.96k
...clinical-stage targeted oncology company committed to... .../ Director, Regulatory Affairs CMC, responsible... ...developing and executing global regulatory CMC strategies across multiple... ...accelerated regulatory submission schedules. Reporting... ...the regulatory CMC lead on cross-functional...RegulatoryFlexible hours- Cacheflow is seeking a Senior Counsel, Regulatory to join our legal team in Bellevue,... ...role provides an opportunity to lead our response to evolving global regulations, focusing on technology... ...include developing compliance strategies and collaborating with product and...Regulatory
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...clinical-stage targeted oncology company committed... .... This role will lead day-to-day... ...Agreements to align with regulatory updates and... ...regulatory submissions, including providing... ...experience leading global regulatory... ...and remediation strategies. Strong understanding...Regulatory- Grant Thornton is seeking a Director, Global Compensation to lead strategy, design, and governance of compensation across our global footprint. You... ...harmonize practices while respecting local markets and regulatory requirements, owning the compensation philosophy, pay structures...RegulatoryLocal area
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The Director of Regulatory Affairs-Software & Systems will... ...compliant, through gaining global market authorization for... ...of regulatory strategies, detailed regulatory plans and submissions. Execute pre-market and... ...development partners and lead/enable strong cross-functional...RegulatoryWork visa- Philips is seeking a Senior Regulatory Affairs Specialist for Ultrasound to collaborate with global regulatory teams and authorities to secure timely product clearances. You will coordinate regulatory submissions (FDA, Health Canada, EU MDR, NMPA, ANVISA), provide strategic...RegulatoryWork at office
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Databricks is seeking a Senior Counsel, Regulatory for our Bellevue office to lead compliance with global regulations. This unique role requires building a new regulatory practice while collaborating with various teams to provide focused legal advice. The ideal candidate...RegulatoryWork at office$222.29k - $294.01k
...clinical-stage targeted oncology company committed... ...understanding of global pharmacovigilance... ...pharmacovigilance strategies in alignment with corporate and regulatory objectives.... ...emerging safety signals, leading benefit-risk... ...sections of regulatory submissions including INDs,...Regulatory$177.81k - $203.99k
...a clinical-stage targeted oncology company committed to developing... ...Control, Biologics to lead QC strategy and execution in support... ...clinical development and regulatory submissions. The successful candidate... ...knowledge of GMP requirements and global regulatory expectations,...RegulatoryContract work$287.89k - $394.94k
...clinical-stage targeted oncology company committed to... ...medical oversight for global clinical studies and serve... ..., Data Management, Regulatory Affairs,... ...and global development strategy of a potentially first... ...preparation of regulatory submissions and health authority interactions...Regulatory
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