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This position is in the Translational Medicine and Clinical Pharmacology department at Sanofi that covers Rare Diseases, Rare Blood Disorders, and Genomic Medicines with a scope that includes small molecule, monoclonal antibody, peptide, nucleic acid, and genomic therapy modalities.
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RN Job Description BLS Core Mandatory Part I (Relias) Core Mandatory Part II (Nursing-Relias) Core Mandatory Part III (Relias) OR RN Skills Checklist Operating Room RN Exam 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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Demonstrates knowledge of pharmacology and safe medication management. Completes discharge assessments: Performs laptop transfer of data twice daily. Tact Staff is seeking a travel nurse RN Hospice for a travel nursing job in Morristown, New Jersey.
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The Clinical Pharmacology and Pharmacometrics (CP&P) team at BMS is responsible for the pharmacology and pharmacometric support for all pipeline assets throughout the clinical development lifecycle.
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Demonstrate knowledge of anatomy, physiology and pharmacology. Opportunities with Optum in New Jersey (formerly Legacy Riverside Medical Group,). Demonstrate knowledge of anatomy, physiology and pharmacology.
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As a Director within the Clinical Pharmacology Neuroscience Group at AbbVie, you will lead clinical pharmacology programs in the Neuroscience/Psychiatry drug development area. PhD with typically 9+ years of experience or PharmD with typically 11+ years of experience in a relevant field (*relevant field includes experience with PK, PBPK, PK-PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters.
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Understand the impact of DMPK/BA and interdependencies with other functional teams within the enterprise including Pharmacology, Toxicology, Clinical and Regulatory disciplines. Partner with Drug Metabolism and Pharmacokinetic (DMPK) and Bioanalytical (BA) Subject Matter Experts (SMEs) to author, review and track regulatory documents.
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The Director will use strong leadership and communication skills to ensure effective collaboration across development functions and sites, and 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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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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PhD Engineering, Mathematics, Bioinformatics, Pharmacometrics, Systems Biology/Pharmacology or a related field with a proven record of productivity as demonstrated by publications and conference presentations required.
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Specific areas of work may include clinical trials for Phase 1, Pharmacokinetics, and Clinical Pharmacology. Specific areas of work may include clinical trials for Phase 1, Pharmacokinetics, and Clinical Pharmacology.
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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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Leading pharmaceutical company looking for a Nonclinical Regulatory and Scientific Writer. Job Title : Nonclinical Regulatory Document and Scientific Writer. At minimum, a Bachelor’s degree in Chemistry, Biology or related science with a strong background in DMPK and BA including knowledge of the FDA GLPs.
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The CP&P team interacts with discovery and translational scientists, project leadership, early and late clinical development teams and commercial colleagues to provide input on clinical pharmacology profiling, dose optimization, formulation bridging, and combination strategies to enable faster and more effective drug development informed by core scientific principals and data.
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Nonclinical Regulatory Document and Scientific Writer. Experience reviewing regulatory documents, DMPK and BA reports, and non-GLP/GLP data and notebooks. Assist with quality review of DMPK reports that are generated by DMPK scientists by fully reviewing the raw data outputs/electronic notebooks and ensuring validity and quality of reported data in the reports, in addition to reviewing DMPK regulatory documents, editing of nonclinical study reports for regulatory acceptance and adherence to company templates, SOPs, DMPK/BA methods, work practices and FDA GLPs, as applicable.
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pharmacology job in Bernards, NJ
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