Global Regulatory Affairs Program Manager, Oncology
Revolution Medicines
Revolution Medicines is seeking a Manager, Global Regulatory Affairs Project Management in Redwood City, CA. This role leads regulatory submission activities and coordinates cross-functional teams across regulatory, clinical, writing, CMC, and safety to ensure timely filings. The ideal candidate has oncology regulatory experience, strong project management skills, and a track record of managing INDs, NDAs, CTAs, and related submissions. #J-18808-Ljbffr Revolution Medicines
$186k - $233k
...a late-stage clinical oncology company developing novel... ...Associate Director, Global Healthcare Compliance... ...implementation, and ongoing management of the compliance... ...healthcare compliance program. This role serves as a... ...across Compliance, Medical Affairs, Commercial, Clinical...SuggestedFull timeLocal area$244k - $305k
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...Medicines is a late-stage clinical oncology company developing novel targeted... ...Opportunity:The Associate Director, Global Regulatory Affairs Project Management is an integral part of the global... ...applications across RevMed programs. The role partners closely with Global...SuggestedFull timeWork at officeLocal area$186k - $233k
A biopharmaceutical oncology company seeks a Director of Clinical Operations in South San Francisco, CA.... ...involves overseeing Phase 1-3 clinical trials and managing all related activities to ensure compliance with regulatory standards. Candidates should possess over 10...Suggested$244k - $305k
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...is a late-stage clinical oncology company developing novel... ...be responsible for the management, development, and oversight of Global Patient Safety operational... ...Medicines’ clinical programs.Participates in the development... ...reports to global regulatory authorities, central IRB...Full timeContract workLocal area$244k - $305k
...is a late-stage clinical oncology company developing novel... ...design, and execution of a global compliance training program for a biotechnology... ...based training aligned with regulatory requirements and industry... ...global training program management. This role will work closely...Full timeLocal area- Revolution Medicines, a late-stage clinical oncology company, is seeking a Global Patient Safety leader based in Redwood City. You will manage safety information collection and reporting for assigned programs, oversee PV CROs, and ensure compliance with global safety regulations...
$164k - $205k
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...Associate Director, Global Patient Safety Operations... ...a late-stage clinical oncology company developing... ...be responsible for the management, development, and oversight... ...Medicines' clinical programs. Develops and... ...safety reports to global regulatory authorities, central IRB...Contract work$186k - $233k
...late-stage clinical oncology company developing... ...Director, CMC Regulatory who will be responsible... ..., and lifecycle management of RevMed’s... ...support RevMed’s global clinical trials, market... ...global CMC regulatory affairs.Experience in CMC... ...development program.Self-driven, proactive...Full timeWork experience placementLocal area- ...digital transformation of organizations globally, and C3 Generative AI, a suite of domain... ...and delivery expertise.Drive co-marketing programs, including joint events, content, and... ...acumen with a track record of driving and managing to measurable revenue outcomes....
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...late-stage clinical oncology company... ...and executing the global compliance strategy... ...clinical development programs and commercial products... ...to applicable regulatory requirements,... ...compliance risk management, supplier oversight... ...Assurance, Regulatory Affairs, Clinical...Full timeLocal area$110k - $185k
...the newest Snorkeler!Payroll, Global Payroll & Compliance... ...Global Compliance & Benefits Manager to own and scale our payroll,... ...employee benefits administration, regulatory filings, bonus and commission... ...employee bonus and commission programs.Partner with Finance, Revenue...For contractorsLocal areaRemote workRelocation package$150k - $189k
...late-stage clinical oncology company developing... ...Opportunity:The Senior Manager, Compliance... ...and Data Analytics Program. This individual will... ...Commercial, Medical Affairs, Clinical Development, Regulatory, Market Access, Patient... ...to grow and expand globally.This role will...Full timeLocal area- ...Trials Hepatitis C Oncology Pharmaceutical Industry... ...Hiring Success Management Talent Acquisition... ...and administration of its global ethics and compliance programs. The CCO will be responsible... ...understanding of the global regulatory landscape, particularly in...
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...a late-stage clinical oncology company developing novel... ..., cardiac, IRT, data management, Pharmacovigilance,... ...clinical development programs. Oversee and drive the... ...knowledge of applicable regulatory, ICH and GCP. Grant Plan... ...Manager experience. Global Project Level Budget...Contract work$186k - $233k
...Medicines is a late-stage clinical oncology company developing novel... ...:The Associate Director of Regulatory Affairs will provide regulatory... ...to clinical development programs in oncology. They will independently... ...and concise feedback to management and project teams,...Full timeWork experience placementLocal area$244k - $305k
...a late-stage clinical oncology company developing novel... ...: Provide management and leadership of one... ...for late-stage oncology programs. Oversee the development of global regulatory therapeutic area and product... ...8 years in Regulatory Affairs including regulatory...Full timeWork experience placementLocal area$244k - $305k
...a late-stage clinical oncology company developing novel... ...Commercial, Medical Affairs, Market Access, Patient... ...controls.Develop, manage, and conduct monitoring... ...improving the Compliance program by proposing... ...and evolving legal or regulatory requirements.The successful...Full timeLocal areaShift work- ...seeking a senior Quality Assurance leader to oversee the Global Quality Systems Monitoring & Excellence program, ensuring governance and continuous improvement of the QMS. You will drive readiness for regulatory inspections and oversee CAPA and escalation processes across...
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