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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. Advanced knowledge of toxicology, pharmacology, safety pharmacology & DMPK.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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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.
$131,000 - $225,400 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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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. 7 or more years of experience within pharmacovigilance, clinical pharmacology, preclinical research, toxicology and/or biomarker validation (especially in industry) required.
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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.
ExpandApply NowActive JobUpdated 14 days ago - 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.
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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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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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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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The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Listing as PI (Principal Investigator) or Sub I (Sub-Investigator) on Clinical Studies for Cosmetics, Personal care and possibly OTC products. It is an excellent opportunity to increase your experience in the clinical testing arena and potentially lead to industry partnerships and or publications.
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It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
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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 9 days ago - UpvoteDownvoteShare Job
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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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Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
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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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toxicologist pharmacology jobs in Bridgewater, NJ
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