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Represent Regulatory CMC on cross-functional development/commercial teams and Regulatory Affairs teams. Participate in the development of the CMC regulatory strategy for biologics submissions.
$85.5 - $87.07 an hourExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Relevant experience includes experience in the pharmaceutical, biotechnology, or CRO industry, partly in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Monitor, Regulatory Affairs, or Quality Assurance.
$75 - $80 a yearExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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Collaborate with US Government Affairs team to identify and develop policy priorities related to commercial market access. Minimum of 10 years of experience in health policy, market access, and reimbursement, including comprehensive knowledge of commercial payment systems and the healthcare regulatory environment.
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Through our “Lifecycle Evidence Strategy”, “Clinical Trial Optimization”, “Medical Affairs” and “Real World Evidence” services, we deliver impact where it matters, from early drug development to commercialization.
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1.1Big Data Support (Exadata, Netezza, ODA, ZFS, GG, DBA)
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Manages all aspects of the Regulatory Affairs functions for a multi-national generic pharmaceuticals company with focus on US FDA regulations. This position advises company management on the Regulatory Affairs matters as requested and when changes occur in the regulatory landscape with potential impact to the business.
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Bachelors degree in Business Administration, Economics, International Affairs, or a related field. Bachelors degree in Business Administration, Economics, International Affairs, or a related field.
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The Speech Language Pathologist is responsible for the evaluation and treatment of individuals with communication and swallowing disorders within the scope of practice as defined by the State Department of New Jersey Division of Consumer Affairs.
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As a management consulting and technology firm focused on transforming global healthcare and beyond, our most valuable asset is our people.
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Genmab is looking for a (Senior) System Manager to help us maintain, develop, and operate our enterprise electronic document management system (EDMS), GenDocs, covering the clinical development, regulatory affairs, CMC, and QA areas in R&D.
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Works closely with Compliance, Legal and Regulatory to ensure that all US Medical Affairs activities and services are fully compliant with Ascendis SOPs and US as well as global regulatory and compliance rules/law.
$400,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Medical Affairs" and "Real World Evidence" services, we deliver impact where it matters, from early drug development to commercialization. Medical Affairs" and "Real World Evidence" services, we deliver impact where it matters, from early drug development to commercialization.
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This role will be reporting to the Associate Vice President, Digital Strategy, and Media with a strong relationship to the Digital Strategy, Direct to Consumer, e-Commerce, Customer Experience, Sales, and Brand teams.
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The Associate will leverage a variety of analytics and visualization techniques to contribute to research, clinical development, drug safety and post-marketing activities. Stays up to date and compliant with the regulatory landscape related to drug safety and data analyses.
$60 - $68.63 an hourFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Job DescriptionJob DescriptionOVERVIEW:NJM Insurance Group (NJM) seeks Associate Actuaries to join our Personal Lines Pricing and Commercial Lines Pricing teams. ROLE AND RESPONSIBILITIES:As an Associate Actuary, you will collaborate with other actuaries and colleagues across the company to solve important business problems.
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affairs job Title: regulatory affairs associate Company: Thermo Fisher Scientific in Lawrence, NJ
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