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Provide safety oversight and pharmacovigilance management to clinical developmentRegulatory Compliance:Work closely with regulatory affairs to ensure compliance with regulatory requirements throughout the development process.
$225,000 - $275,000 a yearRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The firms areas of practice include Government & Regulatory Affairs, Employment Law, Workers Compensation, Personal Injury, and Family Law. Since our founding, the Firm has built a reputation for competent and ethical representation of our clients in matters of Personal Injury, Workers Compensation, Employment & Labor, and Government & Regulatory Affairs.
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A law firm is seeking a Government and Regulatory Affairs Attorney for their Cherry Hill, NJ office. The Government and Regulatory Affairs Attorney will be responsible for representing public sector clients, particularly in the area of local government/municipal law.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Senior Director, Regulatory Affairs CMC. This position will be working across the company's mid-stage, new development pipeline and will be reporting into the VP of Regulatory Affairs.
$225,000 - $255,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The Executive Director of Advertising & Promotion- Regulatory Affairs prescription drug products manages and, if required participates in, the reviews and approvals of advertising and promotional labeling pieces for prescription drugs.
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Represents regulatory affairs in cross functional prescription product promotional review teams as required, participate in development committees for processes and procedures relating to ad promo.
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Minimum of 3 years of experience in regulatory affairs within the pharmaceutical industry, specifically in a role focused on marketing/advertising. Advanced degree or certification in Regulatory Affairs preferred.
$40 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As Regulatory Affairs – Chemistry, Manufacturing and Controls (CMC) Manager, you will be responsible for managing global CMC regulatory activities, from early phase clinical through marketing applications and early lifecycle activities for multiple projects and teams simultaneously.
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You will work with government entities which influence policy making, regulatory affairs, and legislation that benefit from the practice of project management. Bachelor's degree in business, international relations, law or other relevant field.
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Transamerica is organized by lines of business (Life Insurance, Annuities, Mutual Funds, Retirement Plans, and Employee Benefits), which are supported by Transamerica Corporate (Corporate Development; Finance; Internal Audit; Legislative, Regulatory & Policy; Office of the CEO; People and Places; Brand; Corporate Affairs; Risk; and Technology.
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Our attorneys and governmental affairs professionals work on a multi-disciplinary basis in regulatory counseling, litigation, transactional, and government relations matters on a broad array of issues.
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Assist with general activities of the quality department as required, including the maintenance of various files and information systems including customer and copacker specifications, general correspondence and product manuals, label/product QC hold database, and regulatory affairs activities.
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We are looking for a Senior Director of Global Regulatory Affairs CMC to join a leading pharmaceutical organization in the Greater Philadelphia area. Currently hold a title within Regulatory Affairs CMC pertaining to biologic products.
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CCRP - Cert Clin Research Prof (Preferred) or RAC - Regulatory Affairs Cert (Preferred) 2 Years experience in a regulatory role or 4 Years experience in related clinical research role (Required.
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Influence and shape the regulatory landscape and future regulations with support from a more senior regulatory affairs team member. The Senior Manager, Regulatory Affairs will manage the development and execution of biosimilar regulatory strategy; drive submission related activities and achieve timely filings of regulatory submissions consistent with regulatory requirements to achieve short approval times of critical Biosimilars products.
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regulatory affairs jobs in Philadelphia, PA
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