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The Associate Medical Director will continue to improve performance on the existing HRSA service contract, both in terms of cost benchmarks and quality measures benchmarks. The Associate Medical Director is the lead member of the Site Leadership Team overseeing all aspects of the site operations contributing to defining the overall business strategy and direction of the site.
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Fusion has opened the role in Quality Assurance for a Associate Director/Director, Quality Systems (QS). Experience with Veeva Quality Vault eDS/eQS and Compliance Wire eLMS required.
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The Brook is the leader in providing quality mental health and addiction treatment services. In collaboration with the Director of Outpatient, focuses on maintaining census volumes per budget.
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The Associate Director Clinical Portfolio Execution is accountable for the development of the operational strategy for the clinical study and/or a clinical program (s) as well as the end-to-end study management and delivery of all operational activities and budget management relating to assigned clinical studies/programs.
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Ensure the e-QS Veeva Vault is maintained in accordance with current regulatory compliance requirements and meets current corporate quality and business objectives. Ensuring the workflows and documents are aligned in the Veeva Quality Vault.
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In addition, the Associate Medical Director provides clinical expertise and leadership in the design and implementation of new projects and innovations for the site. The Associate Medical Director performs related work as assigned by the Regional Medical Director.
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Reporting to the Global Quality Systems and Compliance organization, the Associate Director, Quality Program Adoption and Communication will play a pivotal role in overseeing global quality initiatives.
$161,755 - $209,330 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Program Director reports directly to the Chair of the Department with secondary consultation from the Associate Dean, Academic Affairs and the Dean. The PMHNP Program Director is responsible for delivering a high quality educational program for students within the program.
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We have an exciting opportunity within US Medical Affairs for an Associate Director in our Patient Access and Quality of Care (PAQ) team. This position is at our Headquarters in Foster City, CA or Parsippany, NJ.The Associate Director, PAQ- Virology will have responsibility for leading the development of Medical Affairs (MA) strategies and Plans of Action (POA) within the Primary Biliary Cholangitis(PBC)/liverTherapeutic Area (TA) for US payers and key accounts.
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Associate Director, GMP Quality Control at Sumitomo Pharma in Boise, Idaho, United States Job Description Associate Director, GMP Quality Control Sumitomo Pharma America (SMPA) is focused on delivering therapeutic and scientific breakthroughs in areas of critical patient need spanning psychiatry & neurology, oncology, urology, women's health, rare disease, and cell & gene therapies.
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As Associate Director/ Director, Quality Engineering, you are accountable for the Development, Execution and Delivery of domestic and international Quality Strategies for Energy Based Devices at Merz Aesthetics.
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The Associate Dean/Director is responsible for the clinical, administrative, and strategic leadership of The Stone Center Counseling Service and its team of counseling professionals committed to promoting the psychosocial growth and holistic wellbeing of Wellesley students and to delivering high-quality professional services responsive to students’ needs.
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Axsome Therapeutics is seeking an Associate Director/Director, Drug Product Technical Operations. Collaborate with cross-functional teams, including within CMC, Regulatory Affairs, Quality Assurance (QA), and Supply Chain, to drive alignment and ensure successful product development and commercial product launch.
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Legend Biotech is seeking Associate Director, Global Strategy & Investigations Owner/Lead as part of the Technical Operations team based in Raritan, New Jersey. Collaborates and ensures alignment with key cross-functional stakeholders and partners (i.e. supply chain, quality, alliance mgmt., finance, operations, MFG leadership and commercial.
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The Associate Director is responsible to complete quality scientific and medical writing as assigned by the Executive Director, Scientific Affairs and maintain oversight of project deliverables.
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quality director jobs Title: associate
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