- Hologic (Marlborough, MA)
- …of our San Diego or Marlborough campus, and are looking for a Regulatory Affairs Manager , responsible for on-market regulatory activities associated with US FDA, ... Manager , Regulatory Affairs (IVD On-Market/Sustaining) San...international regulatory agencies. This position is focused on in vitro diagnostic systems including assay, software and hardware. The… more
- Amgen (Washington, DC)
- …other innovative, driven professionals in this meaningful role. **Companion Diagnostic Regulatory Affairs Manager ** **Live** **What you will do** Let's do this. ... develop and implement regulatory strategies and processes for in vitro diagnostics (IVDs)/companion diagnostics (CDx's). **Key responsibilities:** + Providing… more
- Hologic (San Diego, CA)
- Clinical Program Manager San Diego, CA,...and supports the development of a strong and engaged clinical affairs department. + Recommends and implements ... Clinical Affair group is hiring for a Clinical Program Manager (CPM) here in San...goals and objectives + Excellent working knowledge of GCP, clinical affairs , and regulatory affairs … more
- Abbott (Alameda, CA)
- … data listings for completeness and accuracy; and escalate issues to the Clinical Operations Manager /Study Lead as needed. + Proactively and effectively ... site staff, and clinical management. + Working knowledge of CFR, ICH-GCP, Clinical and Regulatory Affairs + Proficient with Microsoft Suite The base pay… more
- Abbott (Alameda, CA)
- … data listings for completeness and accuracy; and escalate issues to the Clinical Operations Manager /Study Lead as needed. + Proactively and effectively ... site staff, and clinical management. + Working knowledge of CFR, ICH-GCP, Clinical and Regulatory Affairs + Proficient with Microsoft Suite Apply Now… more
- Abbott (Alameda, CA)
- … data listings for completeness and accuracy, and escalate issues to the Clinical Operations Manager as needed. + Participate in cross-functional clinical ... flexible when priorities change. + Working knowledge of GCP, Clinical and Regulatory Affairs . + Proficient with Microsoft Suite. **Travel Requirements** + Must… more
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