- Vanderbilt University Medical Center (Nashville, TN)
- …University Medical Center** : Located in Nashville, Tennessee, and operating at a global crossroads of teaching, discovery, and patient care, VUMC is a community of ... and takes innovative action to achieve planned goals and objectives. + Clinical Patient Documentation (Advanced): Demonstrates the uppermost levels of expertise in… more
- Oracle (Denver, CO)
- …as SQL, with experience in managing healthcare data securely and efficiently. * Data Standards and APIs: Solid understanding of XML, JSON, REST APIs, and ... AI technologies to enhance product capabilities. * Ensure high-quality engineering standards through code reviews, testing, and best practices. * Provide technical… more
- Gilead Sciences, Inc. (Foster City, CA)
- …These activities include but are not limited to ensuring compliant global processes for vigilance/safety reporting, post-market surveillance system, trending of ... device complaints, risk management, and analysis of safety data sets covering Gilead medical device and combination product portfolio. This role will help drive… more
- IQVIA (Durham, NC)
- …equivalent combination of education, training and experience. IQVIA is a leading global provider of clinical research services, commercial insights and ... identification, strategy and management of various devices and their data ingestion modalities in order to meet the endpoint...and welfare and/or other benefits. IQVIA is a leading global provider of clinical research services, commercial… more
- Teva Pharmaceuticals (West Chester, PA)
- …people to make a difference with. **The opportunity** The Senior Manager in Global Regulatory Medical Writing writes and edits clinical regulatory documents, ... regulations + Global regulations and guidelines for document submissions **Compensation Data ** The annual starting salary for this position is between $123,840 -… more
- Teva Pharmaceuticals (West Chester, PA)
- …in Global Regulatory Medical Writing, may write and edit clinical regulatory documents, including submission summaries and other complex documents, provides a ... regulations + Global regulations and guidelines for document submissions **Compensation Data ** The annual starting salary for this position is between $177,680 -… more
- Pfizer (Albany, NY)
- …stakeholders via established triage process + In collaboration with US and/or Global Medical Affairs colleagues, partner with IM/SC Research & Development and ... Global Product Development (GPD) in the identification of potential...(GPD) in the identification of potential sites for Pfizer-sponsored clinical trials, including identification of sites serving under-represented patient… more
- Envista Holdings Corporation (Pomona, CA)
- …characterize engineering requirements with regards to critical performance attributes and clinical relevance. Test Method Development Design and implement new test ... accuracy, reliability, and alignment with evolving technical requirements and standards . Testing, Validation & Manufacturing Integration Plan and execute testing… more
- W. R. Grace (Columbia, MD)
- …This role ensures optimal supplier selection, cost efficiency, and compliance with global regulatory standards . The ideal candidate will have deep industry ... (https://grace.com/people-and-careers/benefits/us-employee-benefits-summary/) Grace, a Standard Industries company, is a leading global supplier of catalysts, engineered materials and fine chemicals.… more
- Houston Methodist (Houston, TX)
- …and advancement of a unified case management model grounded in clinical excellence, throughput efficiency, care transitions, and denials prevention. A champion ... position promotes innovative strategies while fostering interprofessional collaboration across clinical and administrative domains. This position leads enterprise-wide initiatives… more