- BeOne Medicines (Emeryville, CA)
- **General Description:** Reporting to the Head/Director of Clinical Trial Diversity, the Associate Director will operationalize BeOne's clinical trial ... corporate functions to embed diversity into study design and site selection. The Associate Director will build...internal operations under the leadership of the Head of Clinical Trial Diversity + Primary focus is… more
- Abbott (Austin, TX)
- …and liberate more than 500,000 people with diabetes from routine fingersticks. The ** Associate Manager of Clinical Trial Reimbursement** is responsible for ... implementing and managing clinical trial reimbursement processes to secure Medicare and private payer...Informed Consent Forms (ICF) that support IDE, PAS/PMS and single- site clinical trials. + Create study-level Medicare… more
- Boehringer Ingelheim (Ridgefield, CT)
- …and Metabolism (ExpMed - CRM) is currently seeking a talented and innovative Senior Associate Director, Clinical Trial Leader to support our ExpMed team ... development (SoD) to proof of concept (PoC). The (Senior) Associate Director, Clinical Trial Leader...is responsible for steering and directing clinical trial activities, including patient and site engagement… more
- University of Southern California (San Diego, CA)
- …experience/education as substitute for minimum education Minimum Experience: 2 years in on- site clinical trial monitoring. Minimum Skills: Industry ... site engagement. + Serving as a liaison with clinical trial sites regarding their recruitment and...Or Pharmacology Or in related field(s) Preferred Certifications: Certified Clinical Research Associate (CCRA) and/or Certified … more
- Lilly (Indianapolis, IN)
- …**Responsibilities:** + Be accountable for establishing, obtaining and exceeding goals for clinical trial initiation for development programs. + Lead team ... clear communication of progress through the delivery of all clinical site activities. + Prioritize work to...team of direct reports + 5+ years in a Clinical Trial environment + Qualified candidates must… more
- Sumitomo Pharma (St. Paul, MN)
- …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
- Kelly Services (Irvine, CA)
- …analyses and publications + If applicable, as part of a clinical trial , may assist in providing on- site procedural protocol compliance and data collection ... and Clinical FSP is currently seeking a Associate Clinical Research Specialist for a long-term...trial materials + May interface and collaborate with site personnel, IRBs/ECs, contractors/vendors, and company personnel + Assists… more
- Parexel (Austin, TX)
- …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
- 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