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Experience in managing regulatory relations or affairs in financial services, preferably including experience with the Federal Reserve and/or OCC. Serve as a key liaison between the bank and regulatory agencies, leveraging your prior expertise in regulatory relations or affairs.
$85,000 - $140,000Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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The Associate Director Regulatory Affairs - Oncology is located on site at the Billerica, MA facility with domestic and international travel required. The Associate Director Regulatory Affairs - Oncology is responsible for the regulatory strategy development and execution for their assigned projects in the United States, and supporting other North American countries.
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SUMMARY: The Regulatory Affairs Associate will be responsible for overall product safety and regulatory compliance for products. Respond to internal and external product regulatory inquiries, including, e.g., EPA, FDA, OSHA / GHS, DOT, IATA, and IMDG questions.
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This position independently manages relationships with internal (CSPV, Regulatory, Clinical, Medical Affairs, HEOR and other stakeholders to ensure expectations are clearly defined and met across participating teams) and external stakeholders.
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Dorsey & Whitney LLP is seeking an associate with at least three years of experience to join our Boise office to work on mining, real estate, and renewable energy mergers, acquisitions, joint ventures, and other project development and transactional matters in our Regulatory Affairs Practice Group.
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Quality, Regulatory, Industrial, Finance - Basic knowledge of quality, regulatory affairs, GMP and finance guidelines to understand the impacts on the warehouse management. The Warehouse Associate will be responsible for the accurate and timely execution of assigned activities associated with cycle counting, general maintenance, receiving, put away, picking, staging and shipment of orders within a GMP regulated environment.
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Communicate effectively and collaborate cross-functionally with colleagues in research, development (e.g. PK/PD, biostatistics, non-clinical & clinical operations) and regulatory affairs to support drug discovery and development programs.
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ILPD primarily provides legal advice to OPLA Field Legal Operations Headquarters and OPLA field locations; Enforcement and Removal Operations (ERO); Homeland Security Investigations (HSI); and the ICE Office of Regulatory Affairs and Policy (ORAP.
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Interact with document authors, contributors, and reviewers (including members of Biometrics, Clinical Operations, Clinical Development, Project Management, CMC, Drug Safety, and Regulatory Affairs) to acquire necessary input into documents.
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Understanding of PhRMA, OIG, and ACCME guidelines and policies as well as other regulatory, legal, ethics/compliance guidelines/regulations. The Associate Director, for the Oncology Office of Grants and Education (OGE), is responsible for supporting the Head of OGE with the development of medical education plans, assist in providing direction and oversight for all continuing medical education initiatives, and implementing Novartis policies and procedures in alignment with external regulations.
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The Associate Director, US Regulatory Affairs (RA) serves as the regulatory lead on relative Review Committees (RCs), for products in the Rare Disease, Rare Blood Disorder and Neurology portfolio.
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OPEN JOB: Pharma - Associate Director , US Advertising and Promotion , Global Regulatory Affairs - Hybrid. Represents Global Regulatory Affairs (US RA AdPromo) as a member of cross-functional brand and portfolio team review committees (RC), providing regulatory input into the review and approval of US advertising, promotion, disease-state, market access, and press materials.
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The AD partners with other functional leaders in CMC, Regulatory Affairs, Clinical Operation and Quality Assurance in support of the study project teams and ensures timely drug supply for clinical trials.
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Working knowledge of CFR, ICH-GCP, Clinical and Regulatory Affairs. Participate in the interim and final reviews of study data in preparation of regulatory submissions. Assist and conduct clinical monitoring and site management activities, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department procedures, and other applicable regulatory requirements.
$55,200 - $110,400 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Working in collaboration with the Associate Dean of Academic and Student Affairs, Program Directors, and other student services faculty and staff, the Senior Academic Coordinator will coordinate academic initiatives and programs to meet academic degree, accreditation, and regulatory requirements.
$46,806 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago
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