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PhD in cellular biology, immunology, toxicology or similar field. You will apply in vitro advanced cellular systems to help drive our predictive toxicology capabilities, focusing on the development and execution of complex primary cell models to predict potential toxicities of cell therapies to healthy tissues.
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PhD in Toxicology, Pharmacology or related sciences (or DVM) and a minimum of 10-15+ years of industry experience in Toxicology. Strong knowledge and agility in study design and data interpretation and in the integration of Toxicology studies in the drug progression paradigm, as well as in the incorporation of safety endpoints in pharmacology studies.
$265,200 - $439,300 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Key functions outside CMC include Quality, Regulatory, Clinical, Safety, Corporate Program Management, Project Team Leaders, Toxicology, DMPK, Preclinical functions, Budgeting and Forecasting, IP, and others as organization evolves.
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DVM or PhD in toxicology, pharmacology, or related discipline. As the nonclinical safety subject matter expert, you will be responsible for the nonclinical toxicology studies in support of IND submission.
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Communicate effectively and transparently with functional heads within pharmaceutical development and other company stakeholders (Quality, Toxicology/DMPK, A PhD or advanced degree in Pharmaceutics, Chemical Engineering or equivalent with 10+ years of industrial experience.
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PhD, PharmD or equivalent in Pharmacokinetics, Pharmacology, Bioanalytical or related field with at least 5+ years of experience in Clinical Pharmacology, DMPK or related disciplines required. This position reports to the head of clinical pharmacology and toxicology and liaises with clinical development, clinical operations, non-clinical pharmacology and toxicology, and drug discovery to execute activities for advancing the development pipeline.
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A PhD in toxicology, pharmacology, biology, or equivalent scientific discipline is required, with a minimum of 8-10 years of relevant research experience in a pharmaceutical or biopharmaceutical setting.
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Collaborate with cross functional teams including but not limited to Medicinal Chemistry, DMPK, Toxicology, QA, Pharmaceutical Development, Process R&D, Project Management and Regulatory to timely achieve project goals.
$160,000 - $200,000 a yearExpandUpdated Today - UpvoteDownvoteShare Job
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A PhD degree (or a demonstrated equivalent level of expertise) in a relevant field such as environmental science, biochemistry, biostatistics, environmental or bioresource engineering, toxicology, or epidemiology.
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PhD + 5 years' experience in toxicology or other closely related life sciences field, in the industrial or CRO setting, executing, or managing in vivo studies for the purpose of advancing a biological therapeutic candidate into the clinic (BS +11 years or Masters + 9 years will also be considered.
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Excellent quantitative skills and a vision to leverage the science of dosage projection/simulation, quantitative systems pharmacology, mechanistic toxicology risk assessment, and pharmaceutics in a cutting-edge discipline.
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You have earned a bachelor’s or master’s or PhD of Science in toxicology, pharmacology, biochemistry, microbiology, chemistry or related field (required). You have earned a bachelor’s or master’s or PhD of Science in toxicology, pharmacology, biochemistry, microbiology, chemistry or related field (required.
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Master’s degree in Toxicology, Chemistry, Biochemistry, Environmental Science or biological related major; PhD preferred. Master’s degree in Toxicology, Chemistry, Biochemistry, Environmental Science or biological related major; PhD preferred.
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OR BS degree in health-related or scientific field with 7-10 years of experience in pharmaceutical industry, directly related clinical trial experience or experience in areas relevant to drug discovery or development, e.g. epidemiology, toxicology, pharmacovigilance, regulatory affairs.
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PhD in toxicology, pharmacology, biochemistry, molecular biology, or related subject with focus on human health hazard and risk assessment. Invenia Group is partnered with an exciting AI powered clinical stage biotech company, headquartered in the US, who are seeking a Head of Toxicology with strong experience in advancing drug discovery projects into development to take on this newly created role.
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