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Challenging client or team situations are being managed with guidance from Associate Director, with Influencer Marketing Manager and Influencer Marketing Sr. Associate collaborating closely to bring a solutions-oriented approach to these situations proactively.
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The TMF Associate Director/ Director will provide tactical support and strategic guidance on TMF processes, filing conventions, index creation, maintenance, and other. Reporting to the Vice President of Clinical Operations, the Trial Master File (TMF) Associate Director / Director serves a key role, working across the organization for the execution of TMF Operations processes and strategy.
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The TMF Associate Director/ Director will play a pivotal role in creating and maintaining consistency across studies and programs to ensure essential trial documents are appropriately collected, indexed, stored and accessible, while adhering to regulatory and Morphic standards.
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Join Takeda as an Associate Director where you will have extensive expertise and a comprehensive understanding of antibody discovery, optimization through in vitro based methodologies and advancing programs from discovery towards IND. Together with technical proficiency, strong leadership skills and a collaborative, motivational approach are essential for effective team management.
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POSITION SUMMARY: Under the direction and guidance of the Associate Vice President, Career and Digital Strategy, the Senior Director of Industry and Employer Engagement will develop and lead the implementation of a comprehensive strategic plan that drives engagement with industry, including employers, recruiters and alumni in coordination with Academic Affairs, the International Career Center (ICC) and Alumni Affairs.
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Collaborate with the Senior Art Director, Associate Creative Director, Planners, Content Creators, and Marketing Teams in the conception of both high- and low-production campaigns including photo and video.
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Additionally, as the Associate Chief of Staff, you will collaborate closely with the Chief of Staff to provide strategic guidance and operational oversight to the executive office. The Director of CEO Strategic Support occupies a pivotal position dedicated to advancing the CEO’s strategic vision.
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Manages the DFCI Biosafety Communications Program by identifying topics relevant to investigators with biosafety protocols such as upcoming modifications to IRIS for human gene therapy clinical trials and iRIS-IBC for laboratory registrations and any regulatory and DFCI policy updates, training requirements, resources and guidance, and those requested by the Director of Biosafety.
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The Associate Director, Post Award will work with the Director to ensure that appropriate systems and procedures have been established for proper accountability of all sponsored accounts and to develop a cohesive workflow for OSP’s post award functions, to include oversight of invoicing, financial reporting, milestones/deliverables, re-budgets, accounts receivables, cash management, closeout, and the day-to-day functions of post award accounting, monitoring, management and reporting.
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This role is directly responsible for pre- and post-award activities for 2 substantial NIH funded cooperative agreements (with annual budgets over $38M), and directly supervises and provides leadership and guidance for 1 Team Lead/Sr. Grant Managers, 2 Senior Grant Managers (each with their own portfolio), 1 Jr. Grant Manager, a Financial Program Coordinator, and a Financial Assistant managers, a financial associate, and a project coordinator.
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Reporting to the Senior Associate Director, Fund Management the Assistant Director, Fund Management will play a key role in establishing funds in the appropriate systems and working with University Finance and other offices for fund establishment and ongoing donor compliance for established funds.
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Strong knowledge of laws, regulations, and codes relating to healthcare fraud and abuse and regulated pharmaceutical products, specifically anti-bribery/anti-corruption laws and pharmaceutical regulations and guidance.
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Associate Director: Must have minimum of 8 years pharmaceutical industry with 6 years in Regulatory affairs strategy. The Associate Director of Regulatory Affairs Strategy will be responsible for developing regulatory strategies to support clinical development plans, working cross-functionally across the organization.
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The Associate Director, SAM Operations will be responsible for overseeing and optimizing the operational aspects of the SAM Solutions program under the guidance and leadership of Senior Director, SAM Program Office.
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The Associate Director/Senior Manager of Clinical Quality will develop, manage, and improve existing quality systems to ensure appropriate controls for EyePoint in-house GCP and GLP capabilities.
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associate director guidance jobs in Boston, MA
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