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Reporting to the Vice Dean of the School of Medicine, the Office of Academic Affairs (OAA) comprises 8 faculty associate deans and 25 staff members serving a total population of approximately 5,000.
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PhD preferred, Masters/Bachelors acceptable with relevant experience 6 year experience with PhD; 8 years with Masters or bachelor’s degrees Nonclinical / Clinical Regulatory Affairs experience preferred 2 or more years of line management experience preferred Equal Opportunity Employer/Veterans/Disabled An Equal Opportunity Employer.
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Minimum of 5-7 years' experience in a Data Science role (within Regulatory Affairs or Product Safety functions in the FMCG industry is preferred). You will have the experience of working within the fragrance/ FMCG industry in a unique data scientist role within the Regulatory Affairs function.
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Role: Associate Regulatory Affairs. Familiarity with Global Clinical Trial Applications, Marketing Authorizations, Regulations, and Regulatory Guidance, including familiarity with US Certificate of Pharmaceutical Product (CPP) process.
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Partner with Research, Regulatory Affairs, Medical Affairs, Biometrics, Clinical Operations, Safety, Quality Assurance, Product Development, Business Development, and Management to formulate and implement comprehensive clinical trial plans.
$234,000 - $286,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Reports to: Associate Director, Regulatory Affairs. Job Title: Specialist Regulatory Affairs, Pacific Asia. As the professional in the Regulatory Affairs function, the individual will assist teams in the registration of products by preparing documentation needed for registration in EURI/MENAP global.
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Acceptable and independent skills in the area of regulatory affairs such as understanding broad concepts within labeling and implications across the organization and globally; proactively identify issues; offers creative solutions and strategies, including risk mitigation strategies.
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Associate Director, Regulatory Affairs Advertising and Promotion United States - California - Foster City Gilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need.
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Regulatory Affairs or equivalent pharma experience in animal health is required including prior FDA/CVM/EPA interaction. Advanced degree (Doctor of Veterinary Medicine or PhD in relevant discipline) from an accredited institution with a minimum of five (5) years related experience in Regulatory Affairs strategy/execution; or Masters from an accredited institution in relevant scientific discipline with minimum ten (10) years & experience in Regulatory Affairs strategy/execution.
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Our strategists develop solutions for legislative and regulatory advocacy at the state and federal levels, winning campaigns for proactive/defensive ballot issues, and comprehensive public affairs strategy.
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Bachelor’s or Associate’s degree in public affairs, public policy, political science, communications, marketing, or other relevant field. Organizations come to us for public affairs, advocacy, and political programs that persuade constituents and influence decision-makers across the country.
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At Mainspring, the Manager of Environmental Permitting & Compliance will join a team that sits at the intersection of engineering, sales, installation, maintenance, and regulatory affairs to ensure that our facilities and projects comply with all applicable air quality standards and regulations.
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You will serve as the regulatory expert for labeling on the Global Regulatory Affairs subteam to ensure that regulatory labeling requirements are met for assigned products.
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Role : Regulatory Affairs Associate. Direct interaction with RA functions including Regulatory Operations, Submissions Execution, Regulatory Project Management, Strategic Area and other stakeholders such as Project managers, Manufacturing Plants, affiliates, R&D, Technical center & Product Developers.
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Understanding of scientific principles and regulatory/quality systems relevant to drug development. Join Takeda as an Associate Director, Global Labeling Lead where you will be responsible for the development, maintenance, and implementation of Company Core Data Sheets (CCDS) in line with international standards and guidelines.
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