- Abbott (Santa Clara, CA)
- …imaging catheters and software, vessel closure devices and peripheral stents. This ** Regulatory Affairs Manager ** position is an onsite opportunity ... in a technical area + Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.) + Previous experience with PMA / IDE and… more
- J&J Family of Companies (Irvine, CA)
- …Liquid Embolic System and Enterprise Vascular Reconstruction Device with Clinical Affairs , Regulatory , and Legal teams. + Oversee development and progressive ... and specialists, collaborating with multiple cross-functional partners including Marketing, Medical Affairs , Clinical Teams, Regulatory Affairs , and Sales… more
- Abbott (Santa Clara, CA)
- …Opportunity** We currently have an opportunity available for a **Global Endovascular Product Manager ** to join our ** Vascular ** division in **Santa Clara, CA.** ... provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease. The Global Product Manager will manage a portfolio… more
- Abbott (Alameda, CA)
- …manage the digital health analytics + Work cross functionally with market access, regulatory affairs , medical and clinical resources to deliver on critical ... measure, track and analyze glucose levels. We are seeking a Senior Manager , FreeStyle Libre Ecosystem and Strategic Partnerships to drive the commercialization and… more
- Abbott (Santa Clara, CA)
- …with other departments including Global Clinical Operations, Research & Development, Regulatory Affairs , and Biostatistics. + Writes, study protocols, protocol ... regulatory agency meetings. + Works collaboratively with R&D, Clinical R&D, Regulatory Affairs , Library Services, Product Performance Group (PPG), Quality… more
- Edwards Lifesciences (Irvine, CA)
- …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize… more