- 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
- Parexel (Raleigh, NC)
- …quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to ... Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of...the set-up, running and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring… 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
- Parexel (Raleigh, NC)
- …quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to ... Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of...the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:**… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …Oversees the clinical feasibility assessment, strategic planning, and operations of clinical trial programs or studies. Executes on these global programs or ... services in more than 110 countries and regions. The Associate Director of Clinical Operations serves as...Supplies to ensure timely manufacturing, packaging, labeling, shipping of clinical trial supplies for which the incumbent… more
- IQVIA (Durham, NC)
- …may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... IQVIA is hiring a Clinical Research Associate 2 with on- site monitoring experience...site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's… more
- IQVIA (Durham, NC)
- …bring breakthrough treatments to patients faster._ **Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key ... role in ensuring the successful execution of clinical trials. In this position, you will be responsible...essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site… more
- Sumitomo Pharma (Raleigh, NC)
- …clinical research program with minimal direction + Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing ... seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The … 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
- ThermoFisher Scientific (Wilmington, NC)
- …patient recruitment strategies and the implementation of digital and decentralized clinical trial solutions. + Proven experience providing protocol review ... of Patient-First technology solutions, supporting future innovation and advancing patient-centric clinical trial methodologies. At Thermo Fisher Scientific, we… more