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As the Associate Analyst, you'll be a key member of the US Policy & Regulatory Strategy team that develops policy and regulatory positions to support a reliable, affordable, and decarbonized energy future for our electric and gas customers in the Northeast US. National Grid is committed to achieving net zero greenhouse gas (GHG) emissions by 2050 for our operations and the gas and electricity we sell to customers, consistent with our states' climate laws.
$78,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Manage Information Technology applications within Student Affairs, including StarRez (Housing), ARMS (Police), ARMS (Athletics), Campus Groups, ISSM, iModules (with Advancement), Medicat, Advocate (CARE), RAVE, and Titanium.
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The Associate Director of Global Regulatory Affairs Chemistry, Manufacturing, and Controls (GRCMC) will be responsible for leading and providing global CMC regulatory support for the clinical and commercial product portfolio.
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This role is accountable for the planning and technical execution of the CMC regulatory strategy and for representing Regulatory Affairs-CMC in cross-functional teams and with external partners.
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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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As a Principal Regulatory Affairs Specialist at Verily, you will work directly with other Regulatory Affairs team members, partners and a team of experts from diverse fields (e.g., Biology, Chemistry, Physics, Electrical Engineering, Computer Science) to develop, manage and execute regulatory strategies to obtain market clearances for innovative products.
$200,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Work closely with NGS production, Quality and PreClinical Genotox for compliant execution of genotoxicity data packages in support of regulatory filings and clinical programs. Interact with Health Authorities, in writing and verbally, including pre-submission (e.g., pre-IND), scientific advice filings, IND or CTA, meeting briefing books, or other requests from global regulatory authorities.
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Official Title: Admin Asst-Budget Affairs-SJC. Receives direction from the Head Administrative Assistant for Budgetary Affairs in performing duties in accordance with general policies, procedures and internal controls.
$91,425.13 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Ultragenyx is seeking a highly motivated Associate Director Regulatory Affairs CMC, who is inspired to be a compassionate leader in the field of drug development for rare disease patients.
$218,800 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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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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Emerson College, a premier global arts and communication institution with a foundation in the liberal arts, invites inquiries, nominations, and applications for its next Vice President for Student Affairs (VPSA.
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Strong knowledge of and experience working with medical affairs data sets including but not limited to MSL field engagements and KOLS surveys, Medical Information Requests, KOL sentiments, Scientific Communications, Evidence Generation and RWE.
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Proclinical is seeking a Director, Regulatory Affairs for a mid-sized oncology focused biotechnology company with their site in Massachusetts. Report to our Head of Regulatory Affairs and work side by side with your R&D colleagues to develop and execute innovative regulatory strategies for their development programs (from FIH through late-stage clinical programs), including the implementation of non-clinical and clinical regulatory strategy for relevant products.
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A broad understanding of all aspects of CMC including process development, regulatory and quality requirements, analytical development, formulation and drug product technologies, distribution in US/ex-US.
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The Regulatory Affairs Director (RAD), Oncology Cell and Gene Therapy provides strategic regulatory leadership to influence the development of our innovative products across all stages of development.
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Title: regulatory affairs Company: Turnstone Biologics in Waltham, MA
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