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We're seeking a senior scientist with a strong track record of NIH or other multi-year grant funding (as PI or MPI) to serve as Scientific Director in the Advocate Aurora Research Institute.
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Will support HEOR Product Director and Pricing/ Contracting in the development of value-based contracts with external customers. Supports the product director in the timely execution, dissemination, communication and implementation of product-specific US HEOR strategies and tactics in alignment with brand objectives.
$135,000 - $232,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Medical Director for Molecular Oncology will have responsibility for leading clinical research efforts directed towards developing projects that assess the clinical utility of our somatic and circulating tumor DNA testing platforms and establishing the scientific credibility of our test offerings to outside stakeholders in support of our commercial efforts.
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We are looking for an experienced Scientific Leader/Associate Director, Biopharmaceutics to join the US Biopharmaceutics group within Drug Product Development. In this role, you will continue to build biopharmaceutics capability and scientific understanding, and interact with project teams to support the design of all new drug products (including oral, long-acting injectables, implants and biologics) developed within GSK's Pharmaceutical portfolio.
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The Director collaborates with key stakeholders across the company including Training/Medical Excellence, Field-based/ Medical Outcomes Liaisons (MOLs)/Medical Science Liaison (MSL), market access, payer marketing, global medical strategy, and other HEOR team members, to support Insmeds business needs.
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The responsibilities of the Laboratory Director shall include professional, scientific, consultative (or advisory), organizational, administrative, and educational matters relevant to the services offered by the Forensic Toxicology Laboratory.
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An outstanding track record of peer-reviewed publications and/or patent applications that demonstrates technical proficiency, scientific creativity, initiative and the ability to collaborate with others.
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You will be responsible for providing, scientific leadership, and collaborative working environment to advance the drug candidates from IND through Phase IV. In addition, this position will collaborate with cross-functional stakeholders including in vitro & In vivo pharmacology, clinical biomarkers, DMPK, clinical development and operations, regulatory, CMC, and medical affairs.
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PhD (6+ years' experience) or MS (8+ years' experience) in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experience.
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Within this multidisciplinary group, our research leads focus on advancing biomedical research using team-based, open scientific approaches. Have at least 5 years of experience acting as principal investigator or group lead for a scientific program or have postdoctoral experience with a strong publication record.
$134,300 - $201,100 a yearExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Skilled scientist able to discern the advantages and fir fall of a range of analytical techniques such as molecular assays (ddPCR, qPCR, RT-qPCR), flow cytometry, ELISpot, viral assays, cytokine assays, ligand binding assays and Mass SpectrometryIn depth knowledge of concepts such of context of use of fit for purpose assay validation in bioanalysisOverseen assay transfer, scientific quality and study conduct at CRO partners.
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MS, or PhD in Virology, Bacteriology, Immunology, Molecular Biology, Microbiology, Cell Biology, or other relevant scientific fields. Act as a contributing author to high-quality publications describing assay development and/or the immunogenicity and efficacy of candidate and approved drugs in technical, medical, or scientific journals.
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Stay current with scientific advancements and regulatory trends in clinical pharmacology and Pharmacometrics, and apply the knowledge to advance drug discovery and development for the organization.
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The Assistant AD for Strength and Conditioning Coach devises training plans according to sound scientific principles, supervises training sessions, evaluates athletes, maintains athlete records, and teaches strength and conditioning classes as needed.
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CFS uses legal actions, policy initiatives, scientific and policy reports, and corporate and grassroots campaigns to reduce the impacts of industrial agriculture on the environment and human health.
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