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15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs/small molecules.
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Job Title: Sr. Manager of Regulatory Affairs/ In-House Counsel at Software CompanyLocation: Los Angeles, CAEmployment Type: On-site, Full-TimeSalary Range: $135,000-180,000+ Annually Who we are: Software company is a regulatory compliance software company focused on creating better work environments, for everyone.
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Minimum 8-10 years of combined regulatory affairs experience in color cosmetics, both in domestic and international markets. Strong knowledge and expertise in international regulatory affairs and packaging/labeling compliance.
$130,000 - $150,000 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Option 1 : Four (4) years of experience in a regulatory compliance, permit acquisition, occupational health or safety, industrial hygiene, or environmental engineering program. Experience analyzing compliance with regulatory programs related to water, wastewater and/or air quality.
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The Provost's purview includes academic affairs and faculty affairs, admissions and enrollment management, and student affairs and services—allowing the Provost to develop and apply comprehensive strategies that benefit and enrich student experience at Otis. Otis seeks a collaborative leader who is able to inspire and eager to partner, who possesses a wealth of experience in creative research and practice, and whose actions are equitable, respectful, and transparent.
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REQUIREMENTS:A JD and substantial experience (7-10 years) working in the business affairs or business/legal affairs department at a TV, cable or broadcast network, a streaming service, or a production company or entertainment-focused law firm.
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Establish and maintain cross-functional collaborative relationships with internal stakeholders, including R&D, Regulatory, Medical Affairs, Franchise leaders, Market Access at strategic and tactical levels to generate and disseminate robust HEOR findings in support of a broad set of stakeholders including payers.
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Has leadership and management responsibility for overseeing the school's financial and budget administration including budgetary targets; human resources/workforce planning and training including recruitment and development program; information technology; office management; faculty affairs; student affairs; scientific/research affairs; clinical affairs; facilities and space management; fundraising; and compliance with applicable laws and regulations.
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The Accreditation and Licensing Coordinator is responsible for the preparation, coordination, and maintenance of survey readiness and regulatory compliance. Strong knowledge of CIHQ Standards, Title 22, and CMS Conditions of Participation standards and other regulatory agency requirements.
$112,985 - $186,430 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Under general direction of the Legal & Business Affairs department, the Senior Attorney, Marketing is responsible for (1) drafting, negotiating and interpreting contracts, letter agreements and other legal documentation for advertising and marketing services and projects, digital services and media, social media and influencer marketing; and (2) reviewing marketing materials and managing regulatory, statutory, and contractual compliance requirements.
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ARM will also be required to coordinate and communicate cross-functionally within NPC (e.g., Patient Support Center, Customer Engagement, Marketing, Market Access, Public Affairs, State & Government Affairs, Trade, Specialty Pharmacy Account Management, and other applicable third-party affiliates.
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The Associate must reside within territory, or within a reasonable daily commuting distance of 60 miles from territory border. The Access & Reimbursement Manager will serve as the key contact and lead for access and reimbursement support-related matters and is responsible for being the local market access expert on payer policy coverage, multi-channel acquisition pathways, billing and coding, claims processing, reimbursement, and integration of manufacturer support programs into a range of account workflows.
$144,000 - $216,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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KEY RESPONSIBILTIES:Develop strategic direction for Pharmavite’ s regulatory affairs team to include creating functional strategies and specific objectives to support functional infrastructure and the organization as a whole.
$212,585 - $318,878Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Vice Chair of Clinical Affairs will be in charge of directing the work of the clinical team, managing and growing our clinical footprint, oversee ongoing quality assurance tasks, improve and enhance the patient experience and promote standardization and consistency in clinical care pathways across Keck Medicine of USC health sciences campus and radiation oncology satellites.
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Collaborate closely with Music Business & Legal Affairs (BALA) to define parameters of deals for creative music hires. Deep knowledge of the music industry, digital streaming platforms, music publishing, music licensing, record labels, PROs.
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regulatory affairs jobs Title: sr regulatory affairs associate Company: Merck in Los Angeles, CA
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