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Recruitment & Staffing Agencies Verve Therapeutics does not accept agency resumes unless contacted directly by internal Verve Talent Acquisition. EEO Statement Verve Therapeutics is proud to be an equal opportunity workplace and is an affirmative action employer.
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Verve Therapeutics does not accept agency resumes unless contacted directly by internal Verve Talent Acquisition. Verve Therapeutics is proud to be an equal opportunity workplace and is an affirmative action employer.
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We are seeking a motivated Research Associate or Senior Research Associate to join our Formulation Discovery team. Senior Research Associate. Design and preparation of lipid nanoparticles (LNPs) for early-stage evaluation of delivery of nucleic acid payloads in cell-based and preclinical animal models.
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We are currently accepting applications for an Associate Medical Director overseeing Gotham Neighborhood Health Clinics in Queens. The Associate Medical Director will continue to improve performance on the existing HRSA service contract, both in terms of cost benchmarks and quality measures benchmarks.
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The Associate Director, Events will lead and oversee event sales and operations for major client events as well as select internal events for the Academy of Motion Picture Arts and Sciences, the Academy Museum of Motion Pictures, and the Academy Foundation.
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The Translational Oncology (TO) department within the Pfizer Oncology Division is seeking a highly motivated applicant to join our Bioinformatics team as an Associate Director. ROLE SUMMARYThe Translational Oncology (TO) department within the Pfizer Oncology Division is seeking a highly motivated applicant to join our Bioinformatics team as an Associate Director.
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At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases.
$142,500 - $237,500 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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This Associate Director will work with scientists within QP2 by applying one or more of the following pharmacometrics capabilities such as population pharmacokinetics (popPK), PK/PD models, exposure response (ER) models, model-based meta analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into programs and thereby strengthening our pharmacometric capabilities on a continuous basis in decision making and driving pipeline impact.
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The Pharmacokinetics, Dynamics, and Metabolism (PKDM) department at Sanofi contributes to the safe and effective therapeutic treatment of each patient by applying appropriate pharmacokinetic (PK) and pharmacodynamic (PD) principles to drug development and accelerating the process, where possible.
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The Associate Director will perform job duties independently with minimal supervision and/or lead QP2 efforts on drug/vaccine development programs, and author or co-author strategic documents.
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The Associate Director will ensure that collaborative and constructive relationships are maintained with various on-campus departments, such as, but not limited to: academics and compliance (Provost, Deans, & FAR), student-athlete support, student-athlete well-being and life skills programming, financial aid, Title IX , etc.
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With MIDD as an essential component of decision-making at ouor company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. Educational background in pharmacometrics, biopharmaceutics, pharmaceutical sciences, mathematics, statistics/biostatistics, computational biology/chemistry, chemical/biomedical engineering, or a related field.
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Business Intelligence (BI), Database Design, Data Engineering, Data Modeling, Data Science, Data Visualization, Machine Learning, Project Management, Software Development, Stakeholder Relationship Management.
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Knowledge of drug development, pharmacokinetics and pharmacology principles required. The Quantitative Pharmacology and Pharmacometrics (QP2) department drives model-informed drug discovery and development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions.
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Five years or more of post-PhD academic and/or industry experience analyzing and mining large, multidimensional, genomics datasets (e.g. NGS, RNSeq, transcriptomics, proteomics, flow cytometry, etc.) BASIC QUALIFICATIONS Ph. D. or equivalent in computational biology, bioinformatics, biostatistics, computer science, genomics or a related field with postdoctoral research experience in Cancer Biology; or Ph. D. in cancer biology or related field with established advanced capability and track record in developing and applying computational and bioinformatics methods.
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Title: associate director Company: Verve Therapeutics
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