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Reporting to the Director of Finance and Operations, the Grants and Operations Associate will serve as an integral member of the operations team using innovative philanthropy that leverages creativity, innovation, and entrepreneurship to tackle some of the public health sector’s toughest challenges.
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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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Reporting to the Vice President of Development, the Associate Director of Development will play a key role in managing AUA’s fundraising efforts in the United States, including identifying, cultivating, and soliciting high-capacity prospects to make major gifts to the University.
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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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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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Under the general direction of the Associate Vice President, the Director of Enrollment Operations is responsible for the administration of RFU's enrollment operations, software/data information systems (Technolutions Slate and Ellucian Colleague), and communications management.
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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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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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Position Reports to Jenna Walker Associate Director, QA Training & Document Control. 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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Cell Therapy Document Control Specialist. Strong computer skills with MS Office (e.g. Word, Adobe, Visio and Excel) and with Quality Systems (e.g. Document Management System, Quality Management System.
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Manage strategic study operations including: study sites and tracking systems for regulatory submissions, CRO KPIs, drug supply and use, enrollment of subjects, regulatory document flow, study timelines, all budgetary and financial information, Pharmacovigilance/Serious Adverse Events, performance metrics, data flow, etc.
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Maintain required document files and copy to the Area Manager and Director of Operations. Associate degree in Biomedical Engineering Technology, Applied Sciences, degree or certification in Electronics or related field.
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Reporting to the Associate Director of Technology and Support Operations, the selected individual assumes a key role in overseeing, guiding, and harmonizing all endeavors encompassed within the Imaging and Data Processing Unit (IDP.
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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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The Role 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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