- Sumitomo Pharma (Raleigh, NC)
- …Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable ... SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring that… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- … Clinical Research Associate assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ... IVRS set-up, central lab set-up, and other vendor selection processes. + Maintaining clinical trial management system (CTMS) information pertaining to the study… more
- IQVIA (Durham, NC)
- **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director/ Trial Delivery Manager (TDM) to lead and coordinate ... global and regional clinical trial management activities. This role ensures...activities from start-up to close-out. + Escalate and resolve trial issues and contribute to CAPA processes. ** Site… more
- Parexel (Raleigh, NC)
- …quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to ... & North Carolina The Senior Clinical Research Associate (Sr. CRA) is responsible for the site...the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:**… more
- IQVIA (Durham, NC)
- …may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... in accordance with contracted scope of work and Good Clinical Practice. * Work with sites to adapt, drive,...site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's… more
- Sumitomo Pharma (Raleigh, NC)
- …clinical research program with minimal direction + Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing ... a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The medical… more
- ThermoFisher Scientific (Greenville, NC)
- …and supports business development activities. Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic ... modules, etc. to ensure that the medical content is accurate and complete. ** Clinical Trial Support:** + Monitors all safety variables (AE, laboratory… more
- Veterans Affairs, Veterans Health Administration (Greenville, NC)
- …and advanced management of telehealth operations and is typically stationed at a clinical care delivery site (VA Medical Center, CBOC, VA Outreach Clinic, ... Summary The Health Technician (Telehealth Clinical ) - Advanced provides high level support, training,...and maintaining video conferencing connections, making introductions between patient site and provider site , following instructions of… more
- ICON Clinical Research (NC)
- …(Competent Authorities) to obtain all necessary authorizations/approvals pertaining to the clinical trial conduct (start up and maintenance as assigned). ... us on our mission to shape the future of clinical development. **Study Start Up Associate II**...Collect, prepare, review, approve, process and track regulatory and site level critical documents required for study site… more
- ICON Clinical Research (Rocky Mount, NC)
- …specific questions + Review, enter, and edit patient information into clinical trial management software + Book patients into site schedulers ensuring that ... Patient Recruitment Associate - Rocky Mount, NC (Hybrid) ICON plc...where you'll play a key role in transforming the clinical trial experience for patients and sponsors… more