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Key Responsibilities: Lead preclinical studies that provide scientific rationale for advancement to human trials, including safety, efficacy, and mechanisms of action studies using clinically relevant in vitro and in vivo models.
ExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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The Associate Director of Quantitative Science is a self-sufficient and high-impact position that focuses on supporting the statistical and data science needs in the risk-based monitoring (RBM) of clinical trials, serving in roles such as CSM lead (CSM: Centralized Statistical Monitoring), while also support other activities such as preclinical studies, biomarkers, application of AI/ML and development of analysis applications.
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Lead early discovery research from target identification through preclinical assessment, including collaborations with other companies and academia. Alpine seeks a Chief Scientific Officer with a track record of success to enable the company to fully realize its potential for patients, their families and its stakeholders.
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Drive the development of the scientific strategy for the preclinical development of our cancer immunotherapy program, aligning it with the overall corporate objectives and therapeutic goals.
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Be a thought partner providing scientific input for in vivo preclinical toxicology studies. The Toxicologist will collaborate with external vendors, the internal preclinical pharmacology and toxicology team, and other stakeholders across the company to ensure efficient processes that scale with Verve's continued growth.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Partner with other disciplines of integrated drug discovery and development, especially pharmacokinetics and drug disposition, Drug Safety, Regulatory, and Translational Sciences, to develop translational preclinical packages for gene therapy clinical candidates.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Strong scientific foundation, including a strong understanding of preclinical, cardiac, gene therapy products and development. We encourage applicants with strong expertise in AAV gene therapy, experience with IND submission, and particularly those with PharmD or PhD, to apply.
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As part of the Integrated Bioanalysis (iBA) Global Team, you will report to the head of iBA and will be responsible for leading the strategic interface with scientific bioanalytical vendors where you will be responsible for driving a world class collaborative partnership with partners where scientific, regulatory and operational excellence is paramount.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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In addition to a set of advanced programs in the clinic, they have a deep pipeline of wholly owned preclinical candidates, as well as productive collaborations with Merck, AbbVie, Gilead and Bristol Myers Squibb in a broad range of disease areas.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Master’s degree in biology, chemistry, biochemistry, pharmaceutical science, pharmacology, or a related scientific discipline, along with a minimum of 3 years of experience, or a related bioanalysis of clinical and preclinical samples.
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The Clinical Research function, as a sub-function of Scientific Affairs, includes planning, coordinating, and overseeing the successful execution of preclinical and clinical research studies and large-scale data collection efforts in partnership with our surgical practice partners.
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The Research Associate will be responsible for bioengineering, in vitro, and molecular biology assays (RNA sequencing, qPCR, immunostaining) and participate in preclinical animal testing. The Research Associate will design, implement, and lead basic and applied research, development, and scientific research projects independently and in collaboration with the Principal Investigator and other research staff.
$71,650 a yearExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Lead preclinical pharmacology including in vitro and in vivo assay development and execution across the organization. An outstanding track record of peer-reviewed publications and/or patent applications that demonstrates technical proficiency, scientific creativity, initiative and the ability to collaborate with others.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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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 Today - UpvoteDownvoteShare Job
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Interact with the bioanalytical, in vivo teams and customers on scientific study designs, protocols, adverse events, shipping details, and reports. Pharmaron is a premier contract research organization that offers a broad spectrum of R&D and manufacturing service capabilities throughout the entire drug discovery, preclinical, clinical development and commercialization process.
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