- Fresenius Medical Center (Garner, NC)
- …the delivery of maximum quality care to all patients. + Must complete Clinical Manager training modules and ongoing developmental programs within the specified ... requirements. Ensure provision of quality patient care while maintaining cost-effective clinical operations in accordance with all legal, compliance, and regulatory… more
- UNC Health Care (Morrisville, NC)
- …high data quality and integrity by implementing best practices for data validation , cleansing, and monitoring. + **Collaborate with Teams:** Work closely ... development/writer: Advanced - HANA view creation: Advanced - IRB Research/ Clinical Trails/ Research Billing/Documentation development pertaining to data … more
- Fujifilm (Holly Springs, NC)
- **Position Overview** The Manager , QC Virology oversees the QC Virology team, ensuring GMP-compliant laboratory operations in accordance with regulatory guidelines. ... Virus (MMV) testing. As a technical subject matter expert, the Manager provides support for troubleshooting complex investigations and optimizing laboratory systems… more
- Chiesi (Cary, NC)
- …revision, and maintenance of product labelling including the Company Core Data Sheet (CCDS), Target Product Labelling (TPL), United States Package Insert ... documentation to health authorities. + Support regulatory decisions related to Clinical and Global Development programs including Human Factors labelling review in… more
- Fujifilm (Raleigh, NC)
- …+ Firm knowledge of overall network design and security. + Familiarity with clinical data transfer protocols and interfaces (DICOM, HL7, XML, etc.). **Physical ... to oversee all technical aspects of Synapse product implementation, fromsolution validation phases through product go-live. The Project Engineer (PE) must have… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …purpose of this position to act as a team member in the product manager area of Regulatory Affairs (Biopharma) supporting global submissions for various areas of the ... and international regulatory requirements. + Prepare recurrent and routinely requested data , listing, and notifications for assigned projects for submission to… more