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Lead and develop a team of regulatory affairs professionals in areas such as HazCom management, product stewardship, new product development support, labeling reviews, and lifecycle support activities.
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Serve as the main administrative coordinator for the Office of Student Affairs events and work independently to oversee event logistics (including event planning, social media, event promotion, room set-up/clean-up, catering, AV, and IT) and coordinate with departments and offices on main campus and at the law school as needed.
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Understanding of compliance and regulatory requirements for industry medical affairs, R&D and commercial work. Lead the medical affairs strategy congress activity planning in collaboration with team members and compiling of congress reports including critical competitive intelligence.
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Reporting to the Vice President for Student Affairs & Enrollment Management, the Assistant Vice President for Title IX and DHR serves as the senior compliance officer regarding issues of harassment and discrimination at San Francisco State University.
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POSITION SUMMARY Reporting to the Managing Counsel, Health Affairs, Privacy & Data Protection Law, the Principal Counsel - Health Regulatory provides primary legal support to the University's medical centers and health sciences schools on complex and high impact healthcare regulatory analysis.
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Job DescriptionBlock is looking for an experienced Regulatory Licensing Manager with relevant international regulatory lending experience. The core mission of this role is to uphold Block's licensing and other regulatory obligations in the lending space outside of the , which are critical to our success.
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In the position of Regulatory Program Director in Roche / Genentech Pharma Technical Regulatory (PTR), you will be accountable for Health Authority interactions pertaining to CMC Information (i.e.: CMC information in an IND, IMPD and NDA/BLA/MAA filings), as well as informational and pre-submission meetings with global Health Authorities, partners and industry experts.
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Reporting to the Assistant General Manager for External Affairs (EA), the Principal Administrative Analyst, Special Projects is responsible for managing and supporting high-priority projects and initiatives, including providing day-to-day direction and the facilitation and support for executive decision-making.
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Certification in regulatory affairs, quality assurance, or clinical research. Experience conducting training for quality assurance and/or regulatory affairs. Developing, planning, and leading readiness for inspections and audits at CTP by GCP and GxP regulatory authorities, clinical investigator sites, and contract organizations.
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As a Senior Manager, your advanced knowledge of the principles and concepts in the area of regulatory affairs and comprehensive knowledge of other disciplines will enable you to lead complex projects across the division.
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Working with one of my key clients, a clinical-stage biotechnology company dedicated to developing precision medicines for genetically defined neurological and immunological diseases, are looking for an Associate Director, Regulatory Affairs to join their team.
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Maintain knowledge of regulatory environment, global regulations and guidance Contribute to the development and maintenance of Regulatory Affairs working practices and procedures Support in the preparation of the Regulatory Affairs department budget Qualifications, Education & Experience Bachelor’s degree in chemistry, biochemistry, pharmacy, pharmacology, or related scientific discipline required.
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The OpportunityAs an individual contributor, the function of a Senior Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and environment.
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Works with Manager of Legislative Affairs to draft, develop and manage the legislative process for all required department-initiated legislation for Grants, Contracts, Real Estate and other legislative needs, and may directly manage at least one of these portfolios.
$115,934 - $140,894 a yearFull-timeExpandUpdated 2 days ago - UpvoteDownvoteShare Job
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Certification in regulatory affairs, quality assurance or clinical research; ASQ (American Society for Quality) Certification is preferred. Establish and operationalize policies, Standard Operating Procedures (SOPs), and quality assurance processes that ensure program compliance; partner with CRS Compliance and Regulatory Affairs Program to align with existing policies and systems.
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Title: regulatory affairs Company: Biotechnology Innovation Organization in San Francisco, CA
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