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Family planning support up to $45,000 (e.g., IVF/PGT, adoption, surrogacy, egg retrieval) Alloy’s Translational Research team supports our drug discovery partners with in vitro and in vivo testing of therapeutic drug candidates across multiple modalities.
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The ideal candidate will have a deep understanding of healthcare laws as they relate to market access issues such as patient support programs; field reimbursement teams; trade, GPO, PBM and payor relationships and contracts; medical and pharmacy benefit coverage and reimbursement; and drug pricing.
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Certified Substance Abuse Counselor, (CADAC, CAS) or Licensed Alcohol and Drug Counselor (LADC) preferred. Provides support and assistance to clients with legal issues (probation, parole, courts.
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Work collaboratively with the toxicology team and future translational pharmacology and clinical development teams to support the progression of therapies from late discovery through first in human clinical studies integrating DMPK data into the overall drug development strategy.
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This team is searching for a Principal Scientist, ADME. You will be collaborating with the Preclinical and Analytical Sciences group, to manage ADME lab operations and support small molecule drug discovery programs for cardiovascular indications.
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Design, execute and manage in vitro biology functional experiments that support preclinical drug discovery including candidate screening, lead selection, and target validation. Develop fit-for-purpose drug mechanism of action studies which will require bringing novel techniques, assays and/or technology in-house.
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Overview The Dana-Farber Cancer Institute seeks an Executive Assistant to provide varying degrees of executive administrative support to the Center Co-Directors, Scientific Director, and to a limited extent, Center Group Leaders in the newly established Center for Therapeutic Discovery (CTD.
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Provides ad-hoc programming support to Clinical Operations, Data Management, Statistical Programming, Biostatistics, Drug Safety, Clinical Science, Medical Writing and Drug Safety to ensure rapid access to clinical study data for data cleaning/validation, SAS listings review, TLF, dry runs, etc.
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3-5 years relevant experience in academic and/or industry (biotech or pharma) settings including experience in neurodegenerative disease mechanisms, disease modeling, drug discovery or assay development.
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Provides scientific and strategic guidance on stage-appropriate questions related to drug metabolism, bioanalysis, quantitative biomarkers, PK, and PK/PD.Guides efficient design and execution of studies in support of drug candidates.
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Work with medical coding (MedDRA, WHO Drug Global) to ensure coding is performed as per study timeline. Responsible for performing data management oversight activities in support of Leap Clinical Studies by overseeing the activities of the CRO DMs, from study start-up through to study closeout, to ensure adherence to scope of work and service agreements, and that the deliverables are on time, within budget and are of a high quality.
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PepGen is looking for a highly motivated Associate Director or Director level Biomarker scientist who will contribute to the preclinical/clinical development to support and expand their current and future pipeline.
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The Global Genomics team within Translational Medicine function leverages Next Generation Sequencing (NGS) and other advanced technologies to match the right patient to the right drug and support precision oncology approaches for the AZ Oncology pipeline.
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Prior GCP training, knowledge of Good Clinical Data Management practices, and understanding of industry best practices to support drug development programs and submissions through BLA/ MAA are required.
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Understanding of scientific principles and regulatory CMC requirements relevant to global drug development and post-market support. Experience providing strategic regulatory guidance to drug development, registration, and post-market support teams.
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drug support jobs in Cambridge, MA
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