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The Senior Director, GCP Quality Assurance coordinates GCP Compliance activities with Clinical Operations, Regulatory Affairs, Clinical Supply & Logistics, Sample Management and Pharmacovigilance as well as vendors supporting Scholar Rock sponsored Clinical Studies.
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In addition, the Executive Director of CTE provides supervision, leadership and support to ensure that the Instructional Coach has the necessary resources, guidance, and strategic direction to effectively support teachers and improve the quality of CTE instruction.
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The CLIA Quality Manager will collaborate with direct and/or delegated authority to ensure the CLIA Quality Management Systems (QMS) are effective and compliant with applicable requirements, provide leadership and guidance re: CLIA and associated regulations, and support the Lab Director and leadership in maintaining audit readiness.
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Reports all incidents and breaches in the quality of care to the Clinical Pharmacy Manager, Pharmacy Operations Manager or Director of Pharmacy. Director of Pharmacy Operations Manager Clinical Pharmacy Manager Must be able to collaborate and effectively communicate with physicians, nurses and other health care professionals.
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Yes. Direct Reports Include the Director of Member Service, Director of Provider Service, Senior Director of Member Communications, Manager of Training and Quality, Director of Business Strategy and Technology, Director of Member Experience and Improvement, Senior Director of Consumer Affairs, and the Director and Senior Consultant for Consumer Experience.
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Supervise, orient, train, evaluate, and counsel department employees to improve their job performance and to maintain high standards of performance and patient quality care, in conjunction with the Regional Director of Operations and Human Resources.
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Reporting to the Director, Analytical Sciences, this position works closely with other functions in CMC drug development including Drug Product, Drug Substance, Supply Chain, and Quality Control.
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Assist the Director of OCA and Chief of Payment and Care Delivery Innovation with the development and implementation of a holistic strategy for clinical, quality, and analytics initiatives.
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In this role, you will Reporting to the Senior Director, Capital Projects and Project Controls, the Director - Project Controls will be responsible for establishing and implementing project controls methodologies across the company including Front End project execution strategy development, estimating, scheduling, cost control, project buyout and logistics for all Moderna Capital Projects Worldwide.
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As the Director of Master Data Management and Data Governance, you will report to the Sr. Director of Data & Engineering Planning & Governance and be responsible for managing the master data management strategy and technology platforms to support the business and data strategy across all business verticals including Commercial, Clinical, Manufacturing, supply chain, accounting, and finance.
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You and your team of Investment Associates, Performance Analysts, and a Client Service Coordinator are responsible for all client-related activities and quality control of materials for approximately 80-100 different client relationships.
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The Project Director will also support other major implementation, quality improvement, and training initiatives spearheaded by the PIs of the Brain Stimulation and Home-Based Neuromodulation Program, including leading large, multi-disciplinary projects and providing guidance for implementation and program evaluation.
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Performs a variety of technical procedures requiring independent judgement, ingenuity and initiative and maintains quality consistent with established technical standards under the direction of the Chief Technologist, Chief of Radiology, Radiation Safety Officer and the Director of Radiology and Cardiology Services.
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Reporting to the VP of Biometrics, the Director/Sr. Director, Clinical Data Management is responsible for all clinical data management activities related to the effective planning and timely delivery of complete, high quality and reliable clinical trial data.
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Oversee and direct the design and implementation of the CDM process with vendors, including clinical systems design, build and testing, data integration, data review, dictionary coding, data quality checking, data transfer, reporting, and archival activities for EDC, IRT, and other clinical systems.
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quality director jobs in Dorchester Center, MA
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