- Vanderbilt University Medical Center (Clarksville, TN)
- …to provide cancer incidence, treatment, and outcome information. * Submit required data to regulatory and accreditation organizations to maintain compliance ... **Discover Vanderbilt University Medical Center** : Located in Nashville, Tennessee, and...The Tumor Registrar is responsible for all aspects of data collection for reportable cancer cases. The Tumor Registrar… more
- J&J Family of Companies (Irvine, CA)
- …all relevant Clinical R&D partners and cross-functional partners (eg Global Strategic Marketing, Medical Affairs , Regulatory Affairs , Health Economics ... including during sponsor regulatory inspections. + In EMEA, responsible for Regulatory Affairs related tasks associated with clinical trials and evidence… more
- Gilead Sciences, Inc. (Foster City, CA)
- …not only be responsible for delivering best-in-class digital engagement within Public Affairs , but also transform the function into a modern, proactive, insight-led ... development and execution of a global digital communications strategy within Public Affairs , aligning with enterprise brand and business goals. Define the right mix… more
- Sanofi Group (Miami, FL)
- …requested + Plan day-to-day interactions, including discussion points in accordance with Medical Affairs strategy, establishing a frequency of interactions as ... experts and decision-makers engaging in mutual scientific exchanges to accelerate data dissemination. Sanofi's field medical teams enhance the understanding… more
- Vanderbilt University Medical Center (Nashville, TN)
- **Discover Vanderbilt University Medical Center** : Located in Nashville, Tennessee, and operating at a global crossroads of teaching, discovery, and patient care, ... organize and prioritize complex coding work to ensure compliance with regulatory requirements and hospital targets. + Utilize designated coding classification… more
- Zimmer Biomet (Warsaw, IN)
- …of the product development process in compliance with Zimmer Biomet procedures and global regulatory requirements + Supports Regulatory Affairs team with the ... meetings **How You'll Create Impact** + Supports clinical affairs in the creation of clinical study plans and...new product development + FDA QSR and EU MDR medical device regulatory requirements, and industry/ regulatory… more
- Medtronic (Mounds View, MN)
- …be assigned. + Provides leadership for the conduct of clinical studies and for the regulatory affairs function as it applies to product approval. + Studies must ... from key functional groups (Research & Development, Manufacturing, Sales, Marketing, Regulatory Affairs , and European Clinical Groups) to drive clinical… more
- Vanderbilt University Medical Center (Nashville, TN)
- **Discover Vanderbilt University Medical Center** : Located in Nashville, Tennessee, and operating at a global crossroads of teaching, discovery, and patient care, ... quality improvement advisor to provide project management facilitation, education, and data analysis for improvement of systems and processes, under occasional… more
- Weyerhaeuser (Vancouver, WA)
- …reporting as required by government or stakeholders * Monitor compliance * Oversee regulatory reports: extract & gather energy data , calculate, summarize, and ... strategies with them * Monitor and audit energy invoice data against contract terms and prices to ensure we...Partner and assist other departments (legal, risk management, government affairs , etc.) in regulatory interventions * Represent… more
- Sanofi Group (Morristown, NJ)
- …Science), Early Development Clinical Operations (EDCO, including Clinical Trial Managers and Data Managers), Regulatory Affairs , Patients Safety & ... Science), Early Development Clinical Operations (EDCO, including Clinical Trial Managers and Data Managers), Regulatory Affairs , Patients Safety &… more