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3+ years of medical safety leadership experience, inclusive of establishing program-level safety strategy, proactive signal detection & evaluation, risk identification & mitigation planning for early and/or late-stage clinical assets, preparation & authoring of periodic safety reports, Risk Management Plans, health authority responses, and supporting NDA/BLA/MAA submissions.
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Job Description Job Description Axle is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations nationally and abroad.
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BA/BS in Bio/Chem Engineering, Biology, Chemistry, Pharmaceutical Science, Biochemistry, Biophysics, Molecular Biology, Life Sciences, Vaccine Development, or a related scientific discipline.
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Axle is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations nationally and abroad.
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In collaboration with executive leadership, the Executive Director, Medical Affairs will define the Medical Affairs strategy, advance collaborations with key opinion leaders and lays out plans for scientific engagement with health care practitioners, research groups, payers, and patient advocacy groups throughout the company.
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Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products.
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The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
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A minimum of 10 years of experience in a GMP-related industry with at least 7 years of experience in GMP quality assurance in the pharmaceutical or medical device industry. Altimmune (NASDAQ: ALT) is a clinical stage biopharmaceutical company focused on developing treatments for obesity and liver diseases.
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NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
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Experience with industry is a plus, with experience that may include but is not limited to research, CMC, clinical, regulatory, or other relevant roles at biotechnology or pharmaceutical companies, management consulting experience with concentration in Pharma and Biotech.
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Acting as a liaison between DHCA and other County departments, such as the Office of Grants Management, the Office of Management and Budget, the Office of the County Attorney, and the County Executive's Office, and other stakeholders for the internal processing of grant applications.
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You will play a pivotal role in advancing our bioanalytical capabilities through the development of robust and reproducible methods for small and large molecule bioanalysis by LC-MS. You will oversee and support method development efforts, collaborate on LC-MS/MS assay development, and contribute to various aspects of pre-clinical and clinical research.
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Cartesian Therapeutics is seeking a Translational Research Scientist/Senior Scientist with extensive experience in clinical biospecimen analysis to join our team and support translational research related to Cartesians early- to late-stage Clinical Trials.
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Hybrid remote/office work environment - must work at MELE's headquarters office in Rockville, MD three days a week (two days working from home) The company offers technical, engineering, and programmatic support expertise to a host of U.S. federal and international agencies, including, but not limited to, the Department of Energy, the Department of Defense, the Department of Homeland Security, the Department of Justice, INTERPOL, and the International Atomic Energy Agency.
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Minimum 3-5 years clinical experience in any of these areas: acute care, home health, physician office management, managed care organization, provider relations, pharmaceutical sales.
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clinical research pharmaceutical company medical science liaison home office jobs in Gaithersburg, MD
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