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We are seeking an innovative and highly motivated Principal Scientist, Scientific Affairs who will contribute significantly to the development and continued growth of our advanced cell therapy manufacturing platform.
$90,000 - $210,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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OPPORTUNITY Mammoth is hiring a Director/Sr. Director, Regulatory Affairs, Therapeutics, to lead the regulatory activities of our growing CRISPR-based therapeutic programs as we bring them from concept to market.
$205,000 - $260,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Reporting to the Head of Regulatory Affairs, this individual will be responsible for assuring the regulatory strategy is aligned with Health Authority requirements and regulatory submissions are on time and of high quality.
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Partner closely with business functions including Commercial, Medical Affairs, Public Affairs, Government Affairs, Finance and Clinical (amongst others), and other teams as part of the OEC and Legal organizations to address ethics & healthcare compliance policy-related issues.
$200ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Capability in managing deliverables essential for regulatory permit applications, CEQA documents, and environmental due diligence investigations (e.g., wetland delineations, rare plant surveys, habitat assessments, biological resources technical reports.
$150ExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Reporting to our VP of Business & Legal Affairs, Content and Games, you will manage various business and legal affairs for Crunchyroll, with a focus on anime licensing and co-production agreements with Japanese licensors and production committees.
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This is a highly collaborative role and will work closely with The Customer Service, Clinical Operations, Provider Network Operations and Compliance and Regulatory Affairs Departments. Present grievance and appeals data to key stakeholders through Grievance Review Committee (GRC) and the Grievance Program Leadership Team (GPLT) as needed.
$200ExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The optimal candidate participate will lead the department and also collaboratively work across a team of peers in Clinical, Regulatory, Biometrics, Medical Affairs and Commercial and will be accountable for ensuring safety systems, staff and procedures are in place to support a compliant global pharmacovigilance system.
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In addition, the applicant is expected to develop a strong research program, funded by federal and other grants, broadly in the areas of drug development, computational drug discovery and development, or regulatory science.
$250ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Build and maintain an expanded level of knowledge and expertise in CCR model risk management and related supervisory guidance, including existing regulatory requirements and guidance from relevant SR letters, proposed rules and guidance from the U.S. regulatory agencies, and standard methodologies identified during Federal Reserve horizontal reviews.
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Our Client's FDA regulatory group works with broad range of companies, including medical devices, drugs, biologics, diagnostics, digital health, research tools, cosmetics, dietary supplements, wellness products, and other consumer products.
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AA&PI Student Services is part of the Division of Equity & Community Inclusion under Student Affairs & Enrollment Management. Work in collaboration and partnership with other programs, departments, and areas within Student Affairs & Enrollment Management and in Academic Affairs to support Pacific Islander student needs for program planning, course advisement, major and career exploration.
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Consults with Campus Human Resources, Risk Management, Office of Legal Affairs, Academic Units, Academic Affairs, UC San Francisco Police Department, and other UC administrators and departments as appropriate, in resolution of harassment, discrimination, sexual harassment, sexual violence, and retaliation complaints.
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In-depth understanding of CMC regulatory requirements and experience with compiling CMC sections for regulatory filings. This position collaborates closely with cross-functional team members, including analytical development, quality assurance, manufacturing and process development, regulatory and clinical operations.
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Compliance and Regulatory Oversight: Ensure compliance with relevant laws, regulations, and standards (e.g., GDPR, CCPA, SOX, PCI-DSS). Demonstrated experience in risk management, compliance, and regulatory oversight.
Starting at $250ExpandApply NowActive JobUpdated Yesterday
regulatory affairs jobs Title: sr in South San Francisco, CA
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