- 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
- 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
- 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 the successful planning, execution, and closure of clinical trials, whether… 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 ... Midwest, West Coast, Northeast & North Carolina The Senior Clinical Research Associate (Sr. CRA) is responsible...quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites… more
- Cardinal Health (Raleigh, NC)
- …Review agreements in support of various business transactions, including strategic sourcing, clinical trial services, confidentiality, Business Associate and ... information security agreements **_Qualifications_** + 8+ years of experience preferred + JD required; record of high academic achievement in the undergraduate level and in law school preferred + License to practice law in Ohio or active bar license in another… 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. ... in accordance with contracted scope of work and Good Clinical Practice. * Work with sites to adapt, drive,...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 ... a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The medical… more
- Gilead Sciences, Inc. (Raleigh, NC)
- …associated capabilities to support the CDS objectives + Manage quality review of clinical trial documents, workflows, and outputs within the CDS organization to ... ensure clinical trials are conducted in compliance with Gilead procedures,...+ Analyze new regulations and polices with emphasis Good Clinical Practices (GCP) and partner with business experts and… more
- IQVIA (Durham, NC)
- ** Associate Director, Client Services - Clinical Trial Payments** **Overview** IQVIA is a leading global provider of advanced analytics, technology ... and extensive domain expertise. We are currently seeking an Associate Director of Client Services to join our Global...Investigator Payments Delivery team (GIPD). This team supports our Clinical Trial Payments team in streamlining financial… more