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They have gone through sustained growth over the last few years, with an expansion strategy combining both site acquisition and continued investment & development of existing facilities.
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This role will be responsible for development of Health Economic and Outcomes Research (HEOR) strategy and execution of relevant tactics to support the value proposition of Rare Blood Disorders products primarily in hemophilia.
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Reporting to the Vice President, Regulatory Affairs, the Senior Director, Regulatory Affairs – Strategy/Advertising, Promotion and Labeling, is responsible for will be responsible for the development and implementation of our global regulatory strategy.
$260,000 - $270,000 a yearExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Whether you are digitizing drug discovery and development, identifying solutions, or making our work easier and faster, you will be making a difference to countless lives. As an expert and advisor to GBDM and Analytics and Reporting, you will be the primary point of contact in the Pfizer Digital organization for GBDM. The Client Partner will be responsible for all Digital strategy and planning related to GBDM/A&R, including partnering with leaders in clinical to evolve and deliver new digital technologies to advance Pfizer’s Patient First strategy.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Its clients include more than 2,000 biopharmaceutical companies, academic institutions, and regulatory agencies across 62 countriesCertara accelerates medicines using proprietary biosimulation software, technology and services to transform traditional drug discovery and development.
Full-timeRemoteExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Abbvie is seeking a highly motivated and experienced translational scientist to lead a team of senior scientists accountable for driving the development, planning, and execution of the clinical translational research and precision medicine strategy across the rheumatology or gastroenterology drug pipeline at Abbvie.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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7+ years industry experience in oncology drug development. This position willbe responsible foroverseeing clinical trials and the development strategy for multiple medicines in prostate cancer.
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Be the subject matter expert for US drug pricing benchmark data types including WAC, AWP, NADAC, ACA FUL, ensuring our solutions meet customer needs in existing and future commercial data workflows.
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Experience with Jira, Confluence and lean development methodologies is a plus. Be the subject matter expert for US healthcare government and regulatory published drug information and policy data sources (CMS, FDA, etc.
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Serve on cross functional drug product (DP) working group and supports LVV lyophilized DP activities through filing and Process Performance Qualification (PPQ), site characterization plan and execution, tech transfer control strategy, process development, PPQ readiness, PAI (Pre.
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In collaboration with the Assistant Vice President (AVP) of Annual Giving, develop and oversee the digital philanthropy strategy for Miami, including tracking and analyzing campaign results. , which contains information about campus safety, crime statistics, and our drug and alcohol abuse and prevention program designed to prevent the unlawful possession, use, and distribution of drugs and alcohol on campus and at university events and activities.
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Moderna Infectious Disease Development is seeking a motivated and energetic Program Leader with a broad scientific skill base and deep expertise in infectious disease research and development to lead the Cytomegalovirus Vaccine Program Team. The Program Leader will lead a cross-functional team to develop and align stakeholders on the development and regulatory strategy and drive progression of the vaccine candidate through late-phase development, filing, approval, and lifecycle management.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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MS in Pharmaceutical Science with job related experience in the field of drug development and clinical pharmacology. Develops new innovative and impactful clinical pharmacology approaches to processes and drug development strategies and can assemble a multidisciplinary team to execute the components of clinical pharmacology program.
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Medical expert responsible for the development of clinical research strategies and independent direction of Phase 1-3 clinical studies while working with cross-functional project teams (clinical project managers, research, preclinical/clinical pharmacology, biometrics, regulatory, drug safety, CMC), creation and execution of clinical development plans, and the development of strategies that will ultimately lead to approvals of Neurocrine's products.
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Good Understanding of Drug Development and Commercialization of prescription medicines. Ability to understand regulatory implications of product strategy related to labeling development, assessment and management.
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