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Located in Boston, Jnana brings together scientific leaders in small molecule drug discovery and development, a highly experienced management team, and the backing of leading life science investors Bain Capital Life Sciences, RA Capital Management, Polaris Partners, Versant Ventures, Avalon Ventures, Pfizer Ventures, and AbbVie Ventures.
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Deliver: Spearhead drug discovery projects, Design, execute, analyze, and interpret in vitro and in vivo experiments. As a Senior Scientist, you will work within the RNA Medicine team to develop a novel nucleic acid drug development platform.
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A minimum of 2 years of experience in a pharmaceutical industry setting within Drug safety, Pharmacovigilance, or equivalent. Senior Drug Safety Specialist, Compliance - Contract - Cambridge, MA.
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Reporting to the Prior Authorization Supervisor , the Clinical Authorization Specialist is responsible for managing all work related to molecular pathology, high-cost drug, and off-label drug authorizations.
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8+ years’ experience in Drug Safety / Pharmacovigilance in a pharmaceutical or biotech company, CRO or regulatory agency. He/she will need to maintain medical knowledge as required by the role, strong and current knowledge of drug safety and pharmacovigilance regulations, pharmacovigilance practices, safety surveillance and risk-management practices.
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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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The Position The Principal Scientist will provide scientific leadership in the identification and development of novel advanced drug delivery systems to achieve administration (oral, subcutaneous, alternative routes) of biologics including peptides, proteins and other new modalities.
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Approaches that we use to address these issues include molecular biology, virology, cell and tissue culture, drug susceptibility assays, flow cytometry, deep sequencing, and integrated single-cell analyses.
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At 1910 Genetics, we put computation at the heart of drug discovery, blending expertise in computational chemistry, structural biology, pharmacology, genetics, data science, and software engineering to develop drugs for previously undruggable targets.
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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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Practices pharmacy in accordance with laws, rules and regulation of the Massachusetts Board of Registration in Pharmacy, Department of Public Health, U.S. Food and Drug Administration, and Drug Enforcement Administration and in accordance with established departmental policies and procedures.
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Jnana Therapeutics is seeking an exceptional Director/Senior Director, Medicinal Chemist to join our internal chemistry group focused on drug discovery programs for hard-to-drug targets.
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Proficiency in the structure, management, and application of MedDRA and WHO Drug dictionaries across the drug development spectrum (Phase I through post marketing safety data management) and at least one EDC system Experience performing Medidata Rave dictionary upgrades, impact analysis and developing and maintaining coding processes and conventions.
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Experiments will involve the investigation of cancer cell lines, including genetic manipulation, gene expression analyses, protein biochemistry, flow cytometry, drug-response analyses, and mouse transplant assays.
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The individual will join a growing, multidisciplinary team of scientists/engineers and contribute to a variety of in vitro and in vivo activities in a highly collaborative environment focused on drug product translation.
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