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The Senior Scientist functions as a study director to manage the design, execution, analysis, and reporting of pre-clinical discovery research studies across various therapeutic areas. The Senior Scientist is expected to deploy their scientific domain expertise to 1) lead communications with sponsors, 2) interface with business development teams, 3) engage laboratory staff and IACUC, and 4) coordinate with project management and data analysis teammates to manage all aspects of studies from initial pre-clinical study design to final report.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The ideal candidate will be an externally recognized and well respected expert in Clinical Pharmacology, population PK, pharmacometrics, and/or DMPK and have extensive experience applying innovative pharmacology approaches to IND filings, first in human dose prediction, drug development, dose recommendations for clinical studies, study design, dose decisions and health authority interactions.
ExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Act as the lead clinical pharmacologist on clinical pharmacology study teams to support clinical development: independently lead the design, protocol development, execution, analysis, and reporting of clinical pharmacology studies (e.g., food effect, BA/BE, human ADME, drug interactions, renal and hepatic impairment, etc.
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Support DMPK needs for clinical stage programs through close collaboration with Clinical Pharmacology and Toxicology. Work closely with DMPK CROs to design, coordinate, monitor and manage external ADME and PK studies.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Knowledge and experience in pre-clinical in vivo imaging (PET, SPECT, MRI, or CT) including understanding of theory and applying imaging to the study of disease in one or more therapeutic areas to study drug effects, biodistribution, and target engagement.
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The ideal candidate is a Technical Manager with strong experience in study, planning, and design of water and wastewater systems, including familiarity with a broad range of issues related to master planning, treatment and collection/distribution in water or wastewater systems.
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Review preclinical study reports, in conjunction with Pharmacokinetics/DMPK and prepare regulatory submission documentation. Author DMPK, nonclinical toxicology, and biomarker sections of regulatory documents.
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In-depth expertise in test method development, method qualification/transfer, and characterization of small-molecule drugs during preclinical (GLP toxicology) and early-phase clinical development.
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In the lab, we work in a range of systems from basic microbiological culturing of fungi to in vitro infection models and combine molecular biology, genetics, and bioinformatics to study these interactions and their impact on the biology of both host and fungal species.
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Cognito initiated our pivotal study for first-line treatment of Alzheimer’s in Dec 2022 and expects to start additional clinical studies in Mild Cognitive Impairment (MCI) and Parkinson’s Disease in 2023.
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As the Principal Scientist/Associate Director OR Director of Analytical Development, you will help advance pharmaceutical development projects throughout the IND-enabling and clinical development stages of our clients small-molecule protein degraders.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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The team is looking for a highly motivated Research Associate and/or Research Assistant that will be responsible for routine screening of compounds in various in vitro toxicology assays. Responsible for planning and conducting high and low throughput toxicology screens, processing data to a high quality of standards, and within specified time frames.
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Lead Drug Safety and Pharmacovigilance representation in the assigned program team and clinical development team and respective study management teams. Responsible for safety content of IB and ICFs and support of DSMBs or Study specific safety review forums for clinical programs.
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You will be an SME for genotoxicity and gene editing products working closely with Computational Biology, Toxicology, Genomics Innovation and PreClinical Genotox to support the development of genome editing based therapeutics into the clinic.
Full-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Produces Home Study reports and provides recommendations within the specified timeframe. Job Location Childrens Home of Poughkeepsie - Poughkeepsie, NY Remote Type Fully Remote Position Type Full Time Education Level Bachelor's Degree Salary Range $75,000.00 - $80,000.00 Salary/year Travel Percentage National - 50%-75% Job Shift Flex Job Category Nonprofit - Social Services.
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toxicology study jobs in Needham, MA
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