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A PhD, Biology, Pharmacology, Engineering, Pharmacy (Pharm. Draft, finalize, and/or review clinical pharmacology study reports and publications. We are looking for an Associate Director, within our Clinical Pharmacology group.
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An advanced understanding of anatomy, physiology, pathophysiology and pharmacology is required. Morristown Medical Center, Morristown, NJ. On of the following preferred: CCDS, CDIP, CCS. An advanced understanding of anatomy, physiology, pathophysiology and pharmacology is required.
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At Atlantic Health System, our promise to our communities is that anyone who enters anyone of our facilities, receive the highest quality care delivered at the right time, at the right place, and at the right cost.
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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.
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Advanced knowledge of toxicology, pharmacology, safety pharmacology & DMPK. Comprehensive knowledge of GLP regulations and all regulatory guidance related to the nonclinical evaluation. Minimum of 10 years of experience as a regulatory toxicologist (study director/monitor and/or project lead) in the pharmaceutical or biotechnology industry or within a regulatory authority.
$165,000 - $231,667 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Study outputs: Draft responses to IRBs and Health Authorities; Collaborates with Translational Medicine and Clinical Pharmacology to ensure appropriate biomarker, PK / PD measurements; Reviews emerging clinical data regularly; Leads dose-escalation meetings; Performs quality assessment with Delivery Lead e.g. review Tables/Listings/Graphs before database lock and quality check of data; Works with BD&O to ensure SAP update.
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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.
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4 or More Years of experience in the pharmaceutical industry, regulatory agency or academia, with exposure to drug development, clinical pharmacology, and/or epidemiology required. The individual assuming this role may function as a key member of the Global Product Team in collaboration with Clinical Development, Regulatory, Project Management, Biostatistics, Pharmacology, and other departments to strategically manage benefit-risk throughout the lifecycle of the drug.
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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.
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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.
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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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These business functions include: Clinical Operations, Clinical Development, Biostatistics and Data Management, Regulatory Affairs, Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance, Regulatory/Risk Management, Quality Assurance, Medical Affairs, Translational Research, Research, Informatics Services Project Management and Operational Management.
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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.
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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.
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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.
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pharmacology job in Basking Ridge, NJ
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