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Senior Director Clinical Pharmacology will provide leadership and implementation of the clinical pharmacology and pharmacokinetics strategies and initiatives across our early and late-stage clinical programs.
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Develop and implement new clinical pharmacology tools and technologies to drive efficient drug development. Drive execution of clinical pharmacology and quantitative sciences vision through execution, interpretation, and presentation of results to project teams, executive review and decision-making bodies.
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In this position, you will assist with the design and execution of in vivo pharmacology experiments in rodents. Investigate and validate mechanism of action of drug leads by conducting in vivo, ex vivo and in vitro pharmacology experiments.
ExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Experience as Non-Clinical Operations Manager in Pharmacology, DMPK and/or Toxicology. The Non-Clinical Operations Manager will support all nonclinical activities in Pharmacology, DMPK and Toxicology functions for Olema Oncology ranging from early candidate nomination, IND/CTenabling, and NDA/MAsupporting studies.
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The current role is for a Senior Research Associate, Translational Sciences - to join our in-vivo pharmacology team. A BS/BA in Biology, or closely related field with 10+ years of lab experience in in-vivo pharmacology and/or bioanalysis in pharmaceutical environments.
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The candidate will be expected to collaborate with Medicinal Chemistry and Pharmacology to develop and implement studies vital to address key program DMPK issues and successfully advance research compounds into development.
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We are actively seeking a senior patent attorney or patent agent with an advanced degree, preferably a Ph. D., in a life-science field, such as biology, molecular biology, biochemistry, pharmacology, or immunology, and at least 5 years of experience in preparing and prosecuting patent applications.
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What we are looking for in a Scientist I/II, Investigative Toxicology:Bachelors (BS/BA) in pharmacology, pharmaceutical science, biology, bioengineering, chemistry, physiology, or related discipline is required; Masters (MS) degree is desirable, but not required.
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The Department's 17 divisions include Academic General Pediatrics, Child Development& Community Health; Allergy, Immunology and Rheumatology; Cardiology; Environmental Science & Health; Emergency Medicine; Endocrinology; Gastroenterology; Genetics; Genome Information Sciences; Hematology/Oncology; Hospital Medicine; Infectious Diseases; Neonatology; Nephrology; Pharmacology & Drug Discovery; Rehabilitation Medicine; and Respiratory Medicine.
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The Department of Cellular & Molecular Pharmacology (CMP) is a basic science department within the School of Medicine and performs research and training. Advanced computer skills using MAC & PC including proficiency in UCSF financial systems (MyReports, PeopleSoft/RAS, BearBuy and PLUS Faculty Portfolio) and Intermediate-Advanced Excel to produce reports and integrated spreadsheets.
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This position will work in close partnership with colleagues in Clinical Pharmacology, Biostatistics, Nonclinical Development, Bioanalysis, and Biometrics, as well as with external vendors and partners creating an aligned, quantitative framework to impact strategies and decisions on drug development.
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Should have Patent Bar membership and a background in one of the following fields: cell or molecular biology, immunology, biochemistry, bioinformatics, organic chemistry, medicinal chemistry, cancer biology, pharmacology, biophysics, or digital health-focused disciplines.
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PhD in Chemical Biology, Medicinal Chemistry, Pharmacology, or related field. PhD in Chemical Biology, Medicinal Chemistry, Pharmacology, or related field. HTS and phenotypic assay development and screening.
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Implementation of PK-guided dose escalation, early combination strategies and emerging innovations on all Pfizer Oncology first-in-human clinical trials with input from Oncology Research Unit, Oncoloy Regulatory Strategy, Clinical Pharmacology and Precision Medicine, Oncology Clinical Development and Operations, Pharm Sci and Product Teams.
$253,800 - $410,600 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Bachelor's degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields. as part of the Regulatory Affairs Asia Pacific (APAC) team, on-site at our Diabetes Care Division HQ location in Alameda, CA. As an individual contributor, the function of a Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and environment.
$65,900 - $131,900 a yearFull-timeExpandApply NowActive JobUpdated 13 days ago
pharmacology job in Alameda, CA
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