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Working under the Director of the RNA Program and closely with the CEO, you will collaborate with cross-functional teams, including research, manufacturing, product development, clinical development, and regulatory affairs to ensure successful RNA vaccine development.
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Our goal is to build sustainable research capacity that outlasts any single study or funder, empowering African institutions to become global leaders in clinical research and scientific innovation for generations to come.
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Outside of the Platform, the RWE Oncology Lead will work with leaders from Biostatistics & Data Management, Global Regulatory Affairs, Clinical Pharmacology / Pharmacometrics, HEOR, Legal/Compliance, and others to achieve research and business objectives.
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The Platform: The Chief Medical Affairs Office’s Real World Evidence (RWE), VP Lead Oncology is responsible for establishing global scientific leadership and stature through the generation of integrated, end-to-end observational real-world evidence serving all therapeutic areas from proof of concept (POC) trials through LOE for priority pipeline candidates, pipeline supplementation through business development, and marketed inline products.
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This leader will also work across other senior leaders and category aligned RWE teams, RWE Primary and Specialty Care, RWE Clinical Affairs & Clinical Operations, Study Quality Control & Compliance, and RWE Platforms & Partnerships.
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With the Director, RNA Program and AAHI Senior Scientific Leadership, develop and execute a comprehensive strategy for advancing vaccine candidates from preclinical stages through phase 2 clinical trials.
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We seek outstanding candidates with teaching experience in the following: industry experience in entrepreneurship, drug/ medical device development, data science, regulatory affairs, clinical and medical affairs, quality management, project management, finance, business operations, research and development, biometrics, health economics and outcomes research or manufacturing.
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Analytical research and development activities will include literature searches, analytical method development, test procedure writing, analytical method qualification, method transfer, and supportive testing for cross departmental activities.
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Demonstrated scientific knowledge (e.g. GPA) and/or skills to maintain high level of performance. Our client, a world-leading Pharmaceutical Company in Groton, CT is currently looking for a Analytical Chemist I (LC-MS, HPLC) to join their expanding team.
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Our research also deliberately seeks to fill clinical and scientific gaps for civilians worldwide and the U.S. military. Research in a clinical setting (e.g., emergency room, ICU, rehabilitation clinic, physiology clinic, etc.
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Research in the MT Program is guided by the scientific themes of the Program which are to: 1) identify and validate novel therapeutics, targets and pathways for selective tumor targeting; 2) identify cellular/molecular determinants and biomarkers of tumor response; and 3) validate clinical effectiveness of new agents in interventional treatment trials.
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Applicants seeking the rank of Assistant Clinical Professor should demonstrate a track record or promise in teaching and research. Engaging in research and service as defined in the college's Clinical Non-Tenure Track Faculty Manual.
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PK Science is an enterprise-wide organization, working across both Biomedical Research and the Development organizations to advance the scientific knowledge of pharmacokinetics, metabolism and clinical pharmacology.
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The Senior Clinical Research Coordinator will often serve as the primary point of contact within a team of internal and external groups when completing study feasibility reviews and during the study start-up process.
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Director Regulatory Affairs CMC. The candidate should have over 12 years of experience in pharmaceutical/biotech drug development, including more than 4 years in global CMC regulatory affairs, with expertise in PDM development for NCEs/small molecules.
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clinical research scientific affairs jobs Title: director Company: Regeneron Pharmaceuticals Inc
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