- Lilly (Branchburg, NJ)
- …Requirements Planning (MRP) system (SAP) and communications with key business partners.The Clinical Trial Supply Management Associate (CTSMA) is responsible ... innovative supply chain solutions and speed the delivery of clinical trial materials for patients. This is...with CD&OP + As assigned, use forecasting techniques and site inventory management tools to ensure CT Material supply… more
- Cordis (Irvine, CA)
- …solutions that address unmet and critical medical needs. **Responsibilities** We are seeking a Clinical Trial Associate to join our clinical study ... peripheral/coronary space to help execute a randomized, multi-center IDE clinical trial . You will perform various duties...and Study Coordinator meetings + Ensure proper escalation of site /project related issues to the Study Lead in a… more
- Bristol Myers Squibb (Princeton, NJ)
- …decision-making throughout execution. You will apply a strong foundation in both clinical trial science and applied analytics - from understanding protocol ... Lead study optimization analytics, including assessment of patient and site burden, competitive trial landscape, and other...trial strategy is required + Prior exposure to clinical trial delivery processes and data-driven decision… 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 ... Clinical Trial Participant Recruitment Project ManagerApply...sites in their participant recruitment and retention efforts for multi- site clinical trials. The incumbent will be… more
- Lilly (Indianapolis, IN)
- …through philanthropy and volunteerism. **Position Description:** The Trial Capabilities Associate provides clinical trial capabilities in support of ... close-out. The associate is responsible for obtaining clinical trial authorizations and ethical approvals, execution...may be required for the position. Clinical Trial Responsibilities + Initiate investigator site activities,… more
- Highmark Health (Harrisburg, PA)
- …within WPAHS, budget development and contract negotiations. Will configure studies in a Clinical Trial Management System (CTMS), to guide users in accurate data ... MCA billing grid. (5%) + Work closely with the clinical trial billing team to ensure that...or equivalent experience + Experience as a Research Coordinator, Clinical Coordinator, Clinical Research Associate ,… more
- AbbVie (North Chicago, IL)
- …and commercialization of drug development projects. As a member of AbbVie's Clinical Trial Operations Development Program (CTODP), you will participate in ... cross functional teams, including but not limited to data management, regulatory affairs, Clinical Site Management (CSM) and external partners to ensure studies… more
- Abbott (Minneapolis, MN)
- …routine fingersticks. Summary Under the supervision of senior colleague/manager (or delegate), the Associate Clinical Site Lead drives study execution and ... clinical trial enrollment, and ICH-GCP and clinical research application. Adheres to specified site ... clinical staff (eg, operations management, study team, Site Contracts Associate ), as needed. Manage all… 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
- 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, ... set-up, central lab set-up, and other vendor selection processes.** + **Maintaining clinical trial management system (CTMS) information pertaining to the study… more