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Requires a PhD in immunology, molecular biology, or cell biology plus postdoctoral experience (or equivalent relevant experience) with 10+ years’ industry experience in research or drug development.
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In this role, it is expected that the incumbent will represent M&S with cross-functional drug development teams, proactively advocate for model-based approaches, and clearly communicate M&S results.
$184,000 - $276,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Senior Biostatistician is responsible for providing statistical support for drug development programs in all phases of development. PhD in Statistics, Biostatistics, or related field with 5+ years industry experience.
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This leader must have scientific excellence in Translational Immunology with a rich understanding of drug development, leadership, recruitment capabilities, management skills to direct a group of individuals, and excellent communication and collaboration skills to deliver on the therapeutic area strategy.
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3+ years industry experience in drug development or related roles to life cycle management of late stage clinical assets with direct experience of regulatory interactions. MD or PhD degree required; sub-specialty training in Neurology or Immunology is a plus.
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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 3 months ago - UpvoteDownvoteShare Job
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The ASR includes crime statistics and institutional policies concerning campus security, such as those concerning alcohol and drug use, crime prevention, the reporting of crimes, sexual assault, and other matters.
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The Vice President, BioPharmaceutical Development is a strategic leader responsible for oversight of Cell Line Development, Cell Culture Sciences, Purification Sciences, Analytical Sciences and Drug Product Sciences.
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Oncology medical professional with strong experience (at least 9 years if MD, ClinPharm or MD-PhD, at least 15 years if PhD or PharmD) in the pharmaceutical or biopharma industry with clinical development, and/or medical affairs experience.
$299,600 - $499,400 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards.
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The potential candidate is expected to perform various cell and molecular biology techniques, PBMC and exosome isolation from human serum, bioinformatics, in vitro and in vivo experiments to evaluate the combination drug therapy in glioblastoma and the development of biomarkers for pseudoprogression.
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Skills & Requirements:Graduate degree required (PhD, PharmD, MD); MBA preferredMinimum of 12 years related experience in the pharmaceutical industry, with working knowledge of research and development and development operations.
Starting at $250,000 a year (competitive)ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Director of Translational Research and Developmental Therapeutics at the Four Diamond Childhood Cancer Research Center at Penn State University College of Medicine, Hershey, PA, Sinisa Dovat, MD, PhD is currently seeking applications for the Assistant Professor position.
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Strong understanding of clinical pharmacology and pharmacometrics principles and the drug development process. This position is responsible for leading efficient, innovative population PK, PK/PD, exposure-response plan, analysis, interpretation, and reporting to support international drug development programs.
$160,000 - $210,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Comprehensive understanding of regulatory requirements related to drug development, with a keen awareness of current US and EU regulations for therapeutic products. Essential Functions Formulate an operational plan for the development of radioisotope and drug candidates, orchestrating a seamless transition to efficient manufacturing processes involving the identification and implementing optimal manufacturing methods, equipment, and facilities.
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