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Direct the planning and implementation of process development, scale-up, technology transfer, and validation efforts in drug substance manufacturing, ensuring strategic alignment and operational excellence.
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The Principal Toxicologist will be responsible for the design and execution of nonclinical development toxicology studies conducted externally, interpretation and communication of the toxicology data/reports to support drug development decisions, and for summarizing and writing regulatory submissions.
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The Drug Authorization Specialist, with direct supervision of the Prior Authorization Supervisor, is responsible for managing all work related to drug authorizations for all injectable drug treatment plans ordered by Dana Farber Cancer Institute providers using knowledge of payer coverage policies and applies appropriate payer guidelines to all aspects of drug prior authorization work.
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The Senior Manager, Manufacturing Engineering for Drug Substance Drug Product (DSDP) CMC Manufacturing will be a strategic leader building and overseeing a new organization to oversee Vertex’s first of its kind cell therapy combination product, foreseeing the launch of GMP Manufacturing Phase III (Pivotal) and Commercial stage gates.
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Screen patients for basic eligibility into Massachusetts government-sponsored health coverage programs, such as MassHealth, HSN, Health Connector, etc. Assists patients with other eligibility programs, such as Medicare Part D Prescription Drug Coverage through research using Medicare's website; assists patients with the Medicare and MassHealth Open Enrollment periods.
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MD with 10+ years of experience in drug development and drug safety/pharmacovigilance, with specific expertise in clinical oncology, immunology, or genetics. Job Overview: This position is well-suited for a Medical Director with substantial expertise in drug development and safety, providing a unique opportunity to strategize the implementation of safety surveillance for clinical trials, oversee the management of safety signals, take charge of cross-functional teams, and contribute to the development of regulatory safety deliverables.
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Analytical Skill, Analytical Skill, Analytical Thinking, Chemical Biology, Chemistry, Clinical Trials, Collaboration, Communication Skills, Curiosity, Data, Data Analysis, Design Of Experiments, Detail-Oriented, Drug Development, Drug Discovery, Ethics, Gene Therapy, Immunology, Inventory Management, Laboratory, Lifesciences, Machine Learning (Ml), Management, Medical Research, Molecular Biology {+ 10 more.
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We are looking for an Associate Director or Director with several years experience in drug discovery and the biotech/pharma industry, including past experience applying generative AI to small molecule projects.
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Minimum 12 years’ experience as a safety physician with the biotechnology / pharmaceutical industry, leading drug safety & pharmacovigilance, including cross-functional team leadership for signal detection, evaluation, risk classification and management, and communication, for products across multiple stages of development.
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BIOVIA is looking for a motivated Machine Learning Engineer – Drug Discovery to join our Discovery Studio team in San Diego, CA, or Waltham, MA in an onsite/hybrid role. Experience in the development of computational tools for drug design.
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15+ years’ experience in at global pharmaceutical or biotechnology companies, including 10+ years’ experience as a safety physician leading SMT in drug safety & pharmacovigilance for products in clinical trial and post-marketing environments.
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Qualified candidates must have a PhD in synthetic/organic chemistry or related scientific field with 15+ years’ experience in drug substance development and manufacturing and a proven track record in developing and scaling up chemical process to kilo lab, pilot plant and commercial plant scales.
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You possess scientific understanding, particularly in biologics drug discovery, vital for steering product strategy in a science-driven marketplace. 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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Help direct chemistry team(s) at contract research site(s); possess in depth knowledge of medicinal chemistry and the drug discovery process, including lead optimization and DC nomination. Demonstrated strong track record in medicinal chemistry as evidenced by successful advancement of drug discovery projects to clinical candidate nomination.
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This position offers a unique opportunity to work in a dynamic and innovative environment developing your career at the interface of mechanistic research, drug discovery, and preclinical drug development.
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drug screen jobs Title: associate Company: Autonation in Cambridge, MA
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