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Inquiries may be sent to Brenda Coleman, Program Support Specialist for the Rutgers-RWJMS Department of Pharmacology at bcoleman@rwjms.rutgers.edu. The Department of Pharmacology at Rutgers Robert Wood Johnson Medical School (RWJMS) seeks applications for a full-time, non-tenure track faculty position in medical education.
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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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It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
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Janssen Research & Development, LLC is recruiting for an Associate Director, Clinical Pharmacology and Pharmacometrics (CPP) to be located in Spring House, PA, Titusville, NJ or Raritan, NJ. Stay abreast of clinical pharmacology, MIDD, analysis methodology and overall drug development process, including regulatory guidance, and methods in modeling and simulation by engaging with the scientific community (e.g., publishing, presenting at meetings, participating in special interest groups within professional societies, etc.
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Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
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Education Qualifications (from an accredited college or university)- MD Board certification or eligibility requiredExperience Qualifications- 4 or More Years of experience in the pharmaceutical industry, regulatory agency or academia, with exposure to drug development, clinical pharmacology, and/or epidemiology requiredDaiichi Sankyo, Inc. is an equal opportunity/affirmative action employer.
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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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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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Demonstrated knowledge of principles of drug development, pharmacology, clinical trial methodology and design, medical monitoring of trials, assessment of drug risks and benefits, and safety assessment of drugs both on the market and in development and global safety regulations highly preferred.
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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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Master in Pharmaceutical sciences (Pharmacology/Pharmaceutics). 3 to 12 years in reputed pharmaceutical or biopharmaceutical industry with good knowledge about portfolio selection & business development activities.
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As a Senior Director in Pharmacometrics (PPK/PD, QP, or CP as appropriate), this individual will be responsible for managing PMx support for a number of programs in one or more therapeutic focus areas of the development portfolio.
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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.
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Trained in a variety of disciplines, department faculty conduct research in cell signaling and growth control, gene expression, ‘omics approaches to cancer and age-related disease, host-pathogen interactions, the genetic basis of disease, metabolic and liver disease, ion channel pharmacology, cancer and translational pharmacology, therapeutic target development, and drug discovery.
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