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Experience in end-to-end CMC drug development from early to late-stage development, GMP clinical and commercial operations and regulatory submissions. Extensive experience with the process and principles of development, technical transfer, scale up design, drug substance/drug product unit operations, and analytical methods.
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In addition, the role will require the development of strong working relationships within Clinical Development Department and with other key functions including, for example, Pharmacovigilance and Drug Safety, Regulatory, Discovery, CMC, Translational, Trial Operations, Biostatistics and Program Management.
$390,300 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Humana is seeking a Senior Economist to lead the development and management of advanced econometric models to forecast and understand drug utilization trends and costs. Role Responsibilities Advanced Econometric Modeling - designing and maintaining sophisticated time series models that capture the nuanced structures underpinning macro trends in drug utilization and costs by product category, mix, and therapeutic areas, potentially including approaches like VARMAX, UCMs, etc.
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You have a degree in a biological science and are capable of quickly coming up to speed on the biologics drug discovery process. The company facilitates affordable, non-exclusive access to the entire drug discovery community from academic scientists, small and medium biotech, to the largest biopharma.
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We are a market leader in automated bio sample management solutions and genomic services across areas such as drug development, clinical and advanced cell therapies for the industry's top pharmaceutical, biotech, academic and healthcare institutions globally.
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Working knowledge of drug development, clinical research, study design, biostatistics, regulatory, and medical terminology. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Benefits: That is 5 earned paid sick days, Matching 401k plan, Discounted health insurance from United Health Care. Qualifications: BS/BA degree in biochemistry, biophysics or a related discipline with a minimum of 3-5 years industry experience; or a MS degree in biochemistry, biophysics or a related discipline with 2 or more years of industry experience, preferably with a focus on assay development and compound profiling within a drug discovery environment.
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The primary focus of this role is to execute a variety of biophysical assays to help accelerate our drug discovery efforts from exploratory through lead identification and optimization. Qualifications: B.S., M.S. or Ph. D. in Biophysics, Biochemistry, Analytical Chemistry, or related discipline and +2 years of relevant experience in an industrial or academic lab.
ExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Partner with the PL and work with the cross-functional team to drive the drug development process from discovery to preclinical development; Critical to succeeding in this position is an understanding of the drug development process, fluency in the sciences, and a strong ability to organize, prioritize and navigate tasks through challenges inherent in drug discovery/development and alliances.
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This position, with the title to be determined based on your experience, offers an excellent opportunity to work closely with an experienced drug discovery and development team and lead early-stage vector engineering platform development in a fast-paced and highly collaborative environment.
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Our well-proven expertise in medicinal chemistry, custom synthesis, and scale-up process chemistry enables us to support all aspects of drug discovery in a deeply integrated technology-driven platform.
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The Head, GCP Quality Assurance provides strategic leadership and direction for clinical quality assurance operations and other prioritized needs, ensuring Rhythm’s drug development programs comply with regulatory standards and driving continuous improvement of Good Clinical Practices (GCPs.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Strong understanding of the drug development process including strategic and operational aspects from preclinical through lifecycle management. Typically 10-15 years in pharmaceutical/biotechnology industry, including 5+ years in project management, spanning from discovery to clinical development Alliance management experience preferred.
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Job Description Technical expert that will drive process development activities of novel antibody-drug conjugates (ADCs). Experience in design-of-experiments (DoE), quality-by-design (QbD), and development of statistical and mathematical models is a plus.
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Experience:Extensive background in Medical Affairs or broad knowledge about drug development and commercialization. Highly skilled at communicating scientific and clinical information within the drug development environment, including expert use of PowerPoint and other presentation tools.
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drug development jobs in Waltham, MA
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