- Merck (West Point, PA)
- …with the PaCES lead to collaborate with individuals from Clinical Research, Regulatory Affairs , Biostatistics, Outcomes Research, and Operations to ensure COA ... Principal Scientist Patient-Centered Endpoints & Strategy (PaCES) lead, the Senior Scientist has responsibility for coordinating global Clinical Outcomes Assessment… more
- Edwards Lifesciences (Philadelphia, PA)
- …patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you ... Knowledge and understanding of cardiovascular science + Moderate understanding of medical device regulatory requirements and documents, device accountability and… more
- Edwards Lifesciences (Philadelphia, PA)
- …experience working with various internal business partners (especially Sales, Marketing, Clinical, Regulatory , Legal, and Government Affairs staff). + Ability to ... ** Senior Director, US Market Access** Innovation starts from...awareness, our Marketing teams build lasting, trusted relationships with medical professionals and industry stakeholders to ensure patients can… more
- J&J Family of Companies (Spring House, PA)
- …individual clinical project teams as well as functional area partners in Regulatory Affairs , Market Access, Clinical Development, Epidemiology, Commercial Data ... Johnson & Johnson Innovative Medicine is recruiting for an ** Senior Manager, Solid Tumor Oncology, Data Science and Digital Health**… more
- Sumitomo Pharma (Harrisburg, PA)
- …tactics quickly. + Lead cross-functional commercial initiatives across Sales, Market Access, Medical Affairs , and other key functions to ensure alignment, ... are seeking a **strategic** , **experienced** **commercial leader** for the role of ** Senior Director, Orgovyx Brand Marketing Lead** . This is a high-impact and… more
- Capgemini (Pittsburgh, PA)
- …where applicable. + Assist with complaint investigation and documentation interfaces with Regulatory Affairs to support UL, IEC, and FDA submissions. ... Participates in internal audits conducted by internal employees and regulatory agencies. + Develop and execute supplier qualification processes,...a related field. + 8 years of experience in medical device quality engineering or a related field. +… more
- Edwards Lifesciences (Pittsburgh, PA)
- …patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you ... 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… more
- University of Pennsylvania (Philadelphia, PA)
- …wellness programs and resources, and much more. Posted Job Title Senior Application Developer (Institute for Biomedical Informatics) Job Profile Title Application ... Developer Senior Job Description Summary The Supervising Application Developer Sr....and process models, information system metadata, user manuals, and regulatory documentation. + Represent the information system team in… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …by applicable federal, state or local law. Posting Notes: || United States (US) || Pennsylvania (US-PA) || Center Valley || Quality & Regulatory Affairs (QA/RA) ... live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care...activities (desired). + Knowledge of Risk Management practices and regulatory requirements such as FDA QSRs, ISO 13485, ISO… more
- CVS Health (Blue Bell, PA)
- …process development related to pricing and bid development activities, regulatory compliance, competitive analysis, and risk-revenue analysis. The colleague will: ... with business partners to analyze the impact of proposed legislative or regulatory reform and implement required changes in pricing activities. + Collaborate with… more
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