- ICON Clinical Research (NC)
- …forecasted timelines are at risk, and escalate issues as soon as identified. + Preparation , Submission, Review and Approval of Critical Document Package (CDP): + ... II** Responsibilities: + Collect, prepare, review, approve, process and track regulatory and site level critical documents required for study site activation… more
- The City of Rochester, MN (Rochester, MN)
- …conducts financial, statistical, and analytical studies; prepares and assists in the preparation of financial and regulatory reports, statements, and claims for ... *Budget Development/Monitoring + Develop the annual schedule for RPU budget preparation . + Coordinate the development of required budget model components by… more
- Sharp HealthCare (San Diego, CA)
- …position requires the ability to combine clinical/quality considerations with regulatory /financial/utilization review demands to assure patients are receiving care ... level of care.The RN CM I will recommend and document patient classification (status and level of care) for...CM I has accountability for maintaining compliance contractual and regulatory compliance with medical groups as applicable and the… more
- Sharp HealthCare (San Diego, CA)
- …all state and federal regulatory requirements.The RN CM II will develop and document a plan for the day and plan for the stay with patient, family, providers, ... position requires the ability to combine clinical/quality considerations with regulatory /financial/utilization review demands to assure patients are receiving care… more
- ICON Clinical Research (Blue Bell, PA)
- …II and Sr. Site Specialist **Title:** Site Specialist II **Role Summary:** Support preparation , process and tracking of regulatory and site level critical ... and assembling of all documents needed in the Critical Document Package (CDP) and of those required for site...team stakeholders. **Title:** Senior Site Specialist **Role Summary:** Support preparation , process and tracking of regulatory and… more
- Sharp HealthCare (La Mesa, CA)
- …position requires the ability to combine clinical/quality considerations with regulatory /financial/utilization review demands to assure patients are receiving care ... lower level of care.The RN CM will recommend and document patient classification (status and level of care) for...RN CM has accountability for maintaining compliance contractual and regulatory compliance with medical groups as applicable and the… more
- PCI Pharma Services (Philadelphia, PA)
- …Operations, this role ensures that PCI's employment practices, including regulatory adherence, work authorization, policy management, government reporting, and ... programs, and the ability to operationalize HR policies and regulatory requirements across various systems, processes, and teams. **Responsibilities:** **Global… more
- Sanofi Group (Cambridge, MA)
- …Clinical Study Units, and investigators + Develop the clinical part of Briefing regulatory documents, Common Technical Document for submission to regulatory ... leadership of the Global Project Head, with the Global safety Officer, Regulatory Strategist and other key functional representatives to deliver development strategy… more
- Sanofi Group (Morristown, NJ)
- …Study Units, and investigators + Contribute to the clinical part of Common Technical Document for submission to regulatory bodies (FDA, EMA, PMDA etc.) and ... leadership of the Global Project Head, with the Global safety Officer, Regulatory Strategist and other key functional representatives to deliver development strategy… more
- University of Colorado (Aurora, CO)
- …Requisition: #37493** **Job Summary:** **Key Responsibilities:** + Participates in regulatory submissions for Biological License Applications (BLA), filings, and ... communications with regulatory and accreditation agencies including audits including but not...to a patient. + Reviews and assists with the preparation of occurrence (deviation) reports, complaints, and corrective and… more