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Job DescriptionPosition Description:Principal Scientist Translational Pharmacology, NeuroscienceTranslational Medicine at our Research & Development Division is responsible for planning and management of an important inflection point in the drug development process, working closely with scientific, regulatory, statistical, and modelling colleagues across the organization to translate the benchtop science of preclinical discovery into compounds ready for assessment in large clinical populations.
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The Pre-Formulation Scientist I will serve as an integral member of the research team at Cytokinetics. Support preclinical formulation delivery for PK, pharmacology, and toxicology studies to achieve the desired PK coverage in preclinical studies.
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It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
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The Director/Sr. Director of Discovery Pharmacology will drive the strategic planning and execution of drug discovery programs from target validation through clinical candidate selection. The Position Arrowhead is seeking an industry experienced and highly motivated scientist to lead a discovery biology team at its new research and development facility in San Diego, CA. This is an ideal position for an individual with a strong background in drug development who enjoys leading other scientists in a team-oriented, fast-paced, and highly cross-disciplinary environment.
$215,000 - $270,000ExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Funded Postdoctoral Scientist positions are available in Sergei Grivennikov Lab ( at Cedars-Sinai Medical Center in Los Angeles, California. Doctorate Degree (MD, PhD, VMD, or DDS) in biomedical sciences, immunology, pharmacology, or an area directly related to a field of research specialization in broad immunology and/or cancer biology.
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We are seeking an experienced talented scientist to join the Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration.
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Developing and executing model-based analyses including translational PK/PD approaches, population pharmacokinetic models, exposure-response models, clinical trial simulation, disease progression models, quantitative systems pharmacology (QSP) modeling, comparator modeling, thereby strengthening pharmacometrics capabilities on a continuous basis in decision making and driving pipeline impact.
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Business Intelligence (BI), Database Design, Data Engineering, Data Modeling, Data Science, Data Visualization, Machine Learning, Project Management, Software Development, Stakeholder Relationship Management.
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SUMMARY:The Senior Principal Scientist works with a fast-paced team in drug Discovery and Development to provide scientific direction and strategy by being an expert in the design/interpretation of both in vitro and in vivo ADME experiments.
$156,500 - $232,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Ph. D. with 1-3 years of pharmaceutical drug development experience relating to: PKPD, pharmacometrics, mathematics, statistics/ biostatistics, or chemical/biomedical engineering. Masters or PharmD with 3-5 years of experience, where "experience" means having a record of increasing responsibility and independence in a similar role in pharmaceutical drug development.
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To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor. Maintaining a comprehensive understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications (CTDs.
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Masters, with or without PharmD, or equivalent degree with 3-5 years of experience, where “experience” means having a record of increasing responsibility and independence in a similar role in pharmaceutical drug development.
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If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separationpackage, then you are no longer eligible for your separation benefits package.
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Associate Directors are emerging leaders in the field of quantitative drug development, with a developing understanding of the strategic elements of drug development and effective communication skills.
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They collaborate within QP2-IO and with other functional areas, as well as with external vendors and partners, creating an aligned, quantitative framework to impact strategies and decisions on drug development teams.
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