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This position supports three teams within Berklee Academic Affairs—faculty development, graduate studies, and institutional research and assessment—and contributes directly to a broad range of institutional functions including graduate student success, accreditation processes, and faculty and chair professional development offerings.
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External Affairs consists of Communications, Government and Regulatory Affairs, Labor and Workforce Planning, and Community Engagement teams. External Affairs leads Vineyard Offshore’s external presence at the local and state level.
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This internship will provide you with a unique opportunity to gain experience in the field of regulatory affairs and learn firsthand the unique considerations for rare disease development. Reporting Relationship: This person will report to the VP Regulatory Affairs, Medical Writing and Pharmacovigilance.
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Position SummaryThis position is a key leadership role for the development of the In Vivo franchise at CRISPR. Reporting to the Senior Director of Regulatory Affairs CMC, you will work closely with cross-functional teams and partners to bring multiple novel therapies to patients.
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The Director of Student Affairs reports to the Associate Dean of Student Services and collaborates extensively with each of the programs and their different modalities as well as a multitude of university partners.
$141,900 a yearInternExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Participate in CMC project team meetings and provide Regulatory CMC support as needed, including update to the teams on follow-up actions, information request, risk assessment and mitigation in support of clinical trial application and marketing application.
ExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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The Senior Director, Regulatory Affairs will drive global Regulatory strategy for the Spur product development portfolio, advancing clinical stage programs in the gene therapy arena. At least 12 years' experience in regulatory affairs in the gene therapy arena, with evidence of working in development of complex biotechnology/biologicals and/or rare diseases, preferably including small/medium enterprises.
Full-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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Support state level government affairs relations including staying up to date on current issues and trends, assistance in arranging meetings as appropriate and making connections on behalf of the bank.
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The ideal candidate should have a strong background in Regulatory Affairs CMC in a global pharmaceutical and/or biotechnology company with expertise in biologics, deep experience in product development and understanding of US, international regulations, and ICH guidelines related to biologics and cell therapy development.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Join Takeda as a Director, Regulatory Affairs Vaccines CMC where you will provide program leadership and develop CMC regulatory strategy for global vaccine programs in various stages of development.
$266,200 a yearFull-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Under the direction of the Director of Policy and Legislative Affairs, the Deputy Director acts as a liaison between all members of the General Court, as well as all other federal, state, county, and municipal officials and agencies, and the Treasurer and Receiver General.
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The DCAMM Director of External Affairs reports to the Chief of Staff and serves as an important member of the Executive Office team, helping DCAMM contribute to the Administration’s policy and goals related to decarbonization and housing, as well as access and opportunity for underrepresented populations, in addition to supporting the core mission of the agency in real estate, planning, design and construction.
$119,889.17 a yearFull-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Dragonfly Therapeutics is seeking a Head of Regulatory Affairs, title commensurate with experience, and reporting directly to the COO, to lead our Regulatory Affairs organization. Leads, participates and contributes to initiatives and activities to help build a robust high performing regulatory affairs organization including operational excellence for effective and efficient execution.
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Associate Director, Public Affairs will serve as a critical Policy & Advocacy team member with responsibility for relations and collaboration with City and State legislators and regulators who make legislative, regulatory policy, and public policy decisions.
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Provide worldwide regulatory strategy and oversight to ensure Moderna can describe, and support processes required for commercialization of INT products (i.e., neoantigen selection (next generation sequencing and bioinformatics) as well as related to front end specimen collection.
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Title: affairs Company: Turnstone Biologics in Charlestown, MA
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