- Actalent (Irvine, CA)
- Job Title: Project Manager - Quality Assurance in Medical Device IndustryJob Description We are seeking a highly experienced Project Manager to lead Quality ... Affairs (CA), working independently but in alignment with the R&D Program Manager . Responsibilities + Assemble and lead project teams, assign responsibilities, and… more
- Actalent (Irvine, CA)
- Project Manager - Quality Assurance in M&A The position is 100% onsite in Irvine, CA Actalent Services LLC is seeking a highly experienced Project Manager to ... and identify resources to ensure timely project completion. + Capture detailed customer requirements, constraints, and assumptions to define project… more
- GRAIL (Menlo Park, CA)
- …companies. For more information, please visit grail.com The Senior Clinical Data Manager (CDM) will lead data management activities for one or multiple diagnostic ... total work week be on-site. Your specific schedule, determined in collaboration with your manager , will align with team and business needs and could exceed the 40%… more
- Abbott (San Diego, CA)
- …working mothers, female executives, and scientists. **The Opportunity** The **Clinical Trial Manager ** works out of our **San Diego, CA** office location in the ... and quality standards. + Supervise and manage electronic data capture (EDC) systems and electronic trial master file (eTMF)...in diagnostics or medical devices. + Strong knowledge of FDA regulations, including 21 CFR Part 812, 50, and… more
- Danaher Corporation (West Sacramento, CA)
- …which makes everything possible. The Global Commercial Marketing Manager - Microbiology is responsible for driving brand activation ... internal stakeholders (marketing, sales, product management) with external customer expectations. + Capture and integrate Voice of Customer (VOC) and Voice of Sales… more
- Cedars-Sinai (Los Angeles, CA)
- …week, depending on departmental needs. Scheduling will be determined by the hiring manager in alignment with operational priorities. At this time, we can only ... study budget and patient research billing. Ensures compliance with all federal, local, FDA , IRB, and HIPAA guidelines and regulations pertaining to the study and… more
- Terumo Neuro (Aliso Viejo, CA)
- …execution and operational excellence in accordance with ICH Good Clinical Practices, FDA regulations, guidance documents, and company SOPs. Provide oversight of site ... with the protocol, GCP, company SOPs, and all applicable regulations (eg, FDA ). + Understand, read, prepare, and deploy study documentation including, informed… more
- US Tech Solutions (South San Francisco, CA)
- …The Clinical Research Coordinator, under the oversight of the Clinical Trial Manager and PI, is responsible for independently conducting clinical research sessions ... maintaining device accountability, and completing data entry into the Electronic Data Capture (EDC) system. + Maintain Investigator Site Files and support Sponsor… more
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