- ThermoFisher Scientific (Wilmington, NC)
- … study management/oversight, including significant study management support experience (eg clinical trial assistant/ associate or lead CRA). Experience ... Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **CSM ( Clinical Study Manager):** **OBJECTIVES:** **Lead or support study operational… more
- ThermoFisher Scientific (Greenville, NC)
- … study management/oversight, including significant study management support experience (eg, clinical trial assistant/ associate or lead CRA). Experience ... could include either early phase clinical studies or Phase 2 and 3 studies and...priorities and situations * Advanced therapeutic area knowledge and clinical development guidelines and directives * Strong understanding of… more
- 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)
- …associated with the set-up, running and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring Responsibilities and Study ... **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is...quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …IVRS set-up, central lab set-up, and other vendor selection processes. + Maintaining clinical trial management system (CTMS) information pertaining to the study ... **Knowledge, Skills, and Abilities:** Excellent knowledge of medical terminology, protocol, clinical trial process, regulatory requirements, and company SOPs.… more
- Parexel (Raleigh, NC)
- …activities associated with the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:** + Ensure proper ... The Senior Clinical Research Associate (Sr. CRA) is...quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites… 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)
- …applicable, 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...required) 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 ... seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The … 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 File… more