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In addition, the Executive Director reviews, recommends and advises the Associate Vice President on the standards, policies and procedures associated with the successful implementation and execution of complex, overlapping design and construction projects throughout OCP. The Executive director enforces department policies and procedures, establishing and enforcing document and operations QA/QC of all department projects.
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Provide general administrative support, project management, scheduling and document preparation for the Department’s Associate Director of Finance, Associate Director of Operations, Associate Director of People & Workforce, and (as assigned) Vice Chairs, and Associate Vice Chairs.
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The Associate Director of Clinical Quality is responsible for the maintenance of quality processes and procedures that ensure compliance with Good Clinical Practices (GCP) guidance and relevant country regulations.
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The Program Manager position will directly report to the Physician Leader of the Abramson Cancer Center (ACC), Clinical Research Unit (CRU)- Leukemia Research Team and indirectly report to the ACC CRU Associate Director Research Operations.
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Provide administrative support to the onsite management team in their day-to-day operations, assisting with tasks such as data entry, filing, and document preparation. Collaborate with the Lifestyle Director to organize and implement community-wide events, demonstrating flexibility in scheduling as needed.
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The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the BMS Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review and system reporting.
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ORGANIZATION STRUCTURE The Senior Associate, Regulatory Operations/CMC reports into the Manager/ Director, Regulatory Affairs and is based in Morristown, New Jersey. Participate in the development and maintenance of Regulatory Operations systems, processes, checklists and procedures to facilitate consistency 10.
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The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review and system reporting.
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This position will be a key member in the senior leadership team comprising the Vice President of Enrollment Management and Dean of Admissions, Assistant Vice President for Enrollment Management and Executive Director of Admissions, Director of Operations and Technology, Director of Recruitment, Director of the Visitor Center and several Associate Directors.
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This position will serve as a technology partner in the Research and Development (R&D) and Technology Development & Operations (TD&O) domains, providing technology leadership, operational support and project management for key projects.
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The Team Lead for Authoring Support Group will be part of the Global Regulatory Operations group and will develop and manage the authoring support group within Regulatory Affairs (RA) to ensure timely and high-quality document delivery to the Regulatory Publishing Group.
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We are seeking a Clinical Records Associate for our TMF Operations Department Reporting to the Associate Director of TMF Operations. Perform the role of the Clinical Records Associate for all Clinical Trials at 4DMT throughout the TMF lifecycle, from study start-up and document collection to oversight and archiving.
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Oversee the financial aid document imaging process. Manage file document imaging within the office and recordkeeping of all correspondence. Bachelor’s degree preferred or associate degree required.
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The Senior Campaign Operations Specialist is part of the AbbVie Digital Lab and will be responsible for the day-to-day management, oversight and optimization of our Patient Services 1:1 marketing programs reporting to the Associate Director, Campaign Operations.
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Position Reports to Jenna Walker Associate Director, QA Training & Document Control. Cell Therapy Document Control Specialist. Managing an electronic document system for the Cell Therapy Above-Site which includes reviewing and approving document change requests, troubleshooting and releasing documents to an effective state.
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