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Experience with clinical trials regulatory affairs, or related clinical trials experience such clinical research coordinator experience. Under the general direction of the Program Leaders, the Protocol Project Coordinator will provide regulatory administration, project management, and administrative support for the Pediatric Oncology Research Department at the University of California San Francisco.
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Familiarity with the AML/CFT and sanctions regulatory environment for digital assets globally, including the BSA, OFAC and other sanctions regulations, and travel rule requirements. 12+ years of combined in-house/Biglaw experience, including leading regulatory coverage, preferably in fintech, banking, payments, capital markets or other institutional financial services.
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Work closely with the Head of Scientific Affairs & Strategic Partnerships and Scientific Affairs team to produce rapid, thoughtful responses to content-related requests from across Pfizer Oncology (CSO, Medical strategy, BoD, Investor Relations, colleagues, etc.
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Collaboration with all corporate organizations, including senior leadership, Corporate Communications, Governmental Affairs, Media Relations, Electric and Gas Operation and Transmission and Regulatory Affairs.
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The primary role of the Director, Regulatory Affairs - CMC is to create and/or manage contributions from others for CMC regulatory submission documents. This position reports directly to the Senior Director, Head of Regulatory Affairs - CMC. The Director, Regulatory Affairs - CMC will be responsible and accountable for CMC submission documents while successfully up-holding the vision for the function and help mentoring junior team members.
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You Have:3+ years direct experience with federal regulatory examinations (FDIC, FRB, OCC, or CFPB) and bank partnership lending models. You will work with partners in legal, operations, compliance, finance, data analytics and engineering, product and other teams, to ensure that Block is compliant with applicable requirements and obligations while, to the extent possible, streamlining regulatory impact and facilitating innovation.
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The OpportunityThe Associate Director, Regulatory Affairs is responsible for establishing regulatory strategies in coordination with departmental leadership, and independently managing life cycle plans along with regulatory submissions and approvals.
$187 a dayFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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The Global Scientific Affairs COVID & Flu Senior Manager will play a key role in delivering in-house RWE projects and support the development of Vaccines and Antivirals strategy to keep up with the evolving RWE landscape.
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The Provost and Executive Vice Chancellor for Academic Affairs is the chief academic officer for UCCS, providing visionary leadership and strategic direction for all academic programs and initiatives.
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NLIHC seeks a Fund Development Director to work closely with the NLIHC Vice President of External Affairs to support NLIHC’s development and fundraising endeavors. The Fund Development Director will supervise two staff (fund development coordinators) and will themselves report to the VP of external affairs.
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We are looking for a highly analytical, self-motivated, and solution-oriented Biostatistician II with experience and interest in oncology and/or molecular data to join our Tempus Discover team supporting Medical Affairs.
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Drafts and/or provides guidance to the drafting and execution of Verification and Validation test plans in compliance with LifeNet Health (LNH) Quality Systems (QS)/Regulatory Affairs (RA) standards in allograft design and development duties.
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Department members continually work with senior members of Customer Operations, Regulatory and External Affairs, Transmission Operations, Finance, Accounting and outside consultants in performing daily responsibilities and supporting strategic initiatives.
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This incumbent serves as a key member of the site leadership team, and will interact routinely with Manufacturing Management, Operations, R&D, Sales and Marketing, as well as Corporate Quality and Regulatory Affairs.
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Facilitate, oversee, and manage the transfer of Regulatory Affairs documents to Veeva Vault Document Management Modules. Regulatory Affairs Assistant. Assess the acceptability of regulatory documentation to comply with FDA regulatory requirements.
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regulatory affairs jobs Title: principal Company: Parexel
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