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7 or more years of experience within pharmacovigilance, clinical pharmacology, preclinical research, toxicology and/or biomarker validation (especially in industry) required. Grow CSPV's connection to toxicology (MSRL) and Precision Medicine beginning at the start of preclinical development.
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Advanced knowledge of toxicology, pharmacology, safety pharmacology & DMPK. In this role, you will represent toxicology at cross-functional project teams, strategize nonclinical safety data package, oversee safety pharmacology and toxicology studies, author nonclinical sections in regulatory submission documents, and address regulatory inquiries.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Designs and develops clinical studies and research plans in support of asset strategy with the Early Clinical Development Leadership team; clinical studies include first-in-human Phase I, proof of concept Phase I/II, entry registrational studies, biomarker qualification studies, and/or clinical pharmacology studies.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Interact with Medical Directors, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing, and others to design and analyze clinical trials.
Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Insmed is seeking a part-time scientist for the pre-clinical in vivo pharmacology group with prior experience in the maintenance and breeding of highly sensitive genetically modified mouse strains.
Part-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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An advanced understanding of anatomy, physiology, pathophysiology and pharmacology is required. On of the following preferred: CCDS, CDIP, CCS. An advanced understanding of anatomy, physiology, pathophysiology and pharmacology is required.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Solid knowledge of preclinical oncology research methodology to enable interpretation of preclinical data for devising clinical hypotheses and clinical planning purposes. They may also assist on early stage programs, and work closely with the VP of Early Phase Development and the R&D line function on preclinical programs to ensure appropriate planning for the filing of INDs to become the clinical program lead on first in human (FIH) studies for these molecules.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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The candidate will have a medical degree or a PhD in a life-science area like Biology, Immunology, Pharmacology, etc. Support the different functions within the Clinical Team with his/her expertise and leadership (monitoring, data management, biostatistics, medical writing, pharmacovigilance, regulatory affairs) as well as interact with and support Project team members, Clinical Immunology Laboratory, Budget and Planning Functions, Legal and Patent Department, Product Brand Leader and Medical Affairs.
Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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PhD in pharmacology or pharmaceutical sciences or PharmD with a clinical pharmacology research fellowship required. Responsible for all aspects of Clinical Pharmacology and Biopharmaceutics studies and model-based drug development plans, serves as QCP subteam leader / clinical pharmacology project team representative, supports Phase 2/3 clinical pharmacology objectives with high-level supervision, participates in due-diligence activities, and represents global function on study and project teams.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Senior Manager carries out the strategic direction of a program from preclinical through commercialization by driving the development and implementation of integrated project/program plans, goals, budgets, and timelines.
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At least 3 years of experience in all types of non-clinical studies (pharmacology, pharmacokinetics, toxicology, etc.) At least 3 years of experience in all types of non-clinical studies (pharmacology, pharmacokinetics, toxicology, etc.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Plays a key role in the interactions with regulatory authorities (e.g., FDA, EMEA meetings). Provides scientific input to the core documents for the project (e.g., product strategy documents, protocols, submissions, etc.
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RN Job Description ACLS BLS Core Mandatory Part I (Relias) Core Mandatory Part II (Nursing-Relias) Core Mandatory Part III (Relias) Labor & Delivery Skills Checklist Labor And Delivery RN NRP RN Pharmacology About ARMStaffing As recent winners of the 2023 Top Workplaces Award & SIA's Largest Staffing Firms in the US Award, ARMStaffing is a leader in the healthcare staffing industry.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Managing external studies for ADME/PK, toxicology, pharmacology, and translational sciences. Managing external studies for ADME/PK, toxicology, pharmacology, and translational sciences. Lexicon is a biopharmaceutical company with a mission of pioneering medicines that transform patients' lives.
ExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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The successful candidate will provide quality expertise to manage and improve processes across Aquestive's development program, ensuring compliance with Good Clinical Practices (GCP), Good Laboratory Practice (GLP), Preclinical stage and GMP for clinical manufacturing oversight.
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pharmacology preclinical jobs in Basking Ridge, NJ
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