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Reporting to the Chief Medical Officer, the Vice President, Pharmacovigilance will be responsible for providing medical oversight for the global drug safety and pharmacovigilance function to ensure proactive and timely benefit-risk assessments of all safety data, related to our portfolio of autoimmune disease and drug-device combination therapies.
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Drives and implements the Oncology Research strategy in a particular area of research in concordance with the overall Oncology precision drug development strategy; The Oncology Research Portfolio Lead will have global responsibility to drive strategy in target identification to contribute to a competitive and sustainable early research portfolio and deliver preclinical candidates in Oncology as defined by the Oncology precision drug development strategy in select areas of research.
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Facilitate the Drug Development Leadership Team, chaired by the President of R+D. Planning and tracking activities in lead optimization, pharmacology, toxicology, and ADME studies, preclinical work for patient selection and indication expansion, drug supply, formulation development, clinical planning, and operations.
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YOUR TASKS AND RESPONSBILITIESThe primary responsibilities of the Research Oncology Portfolio Lead are to:Drives and implements the Oncology Research strategy in a particular area of research in concordance with the overall Oncology precision drug development strategy.
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The company facilitates affordable, non-exclusive access to the entire drug discovery community from academic scientists, small and medium biotech, to the largest biopharma. You have a minimum of 8-10 years of experience and a strong understanding of antibody and early drug discovery and development.
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We are a dynamic and innovative oncology-focused biopharmaceutical company, seeking a highly motivated individual to join our clients team as Vice President, Drug Safety & Pharmacovigilance.
$375,000 - $425,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The candidate will have the opportunity to lead multi-disciplinary drug discovery and preclinical teams as targets progress and will be expected to work seamlessly with colleagues across discovery research, chemistry, preclinical pharmacology, toxicology and analytical development.
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If you're excited by the challenge of putting protein motion at the heart of drug discovery and passionate about making a difference in the lives of patients, join us! Relay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process with the goal of bringing life-changing therapies to patients.
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Facilitate the Drug Development Leadership Team, chaired by the President, R&D. Plan and track activities in lead optimization, pharmacology, toxicology, and ADME studies, preclinical work for patient selection and indication expansion, drug supply, formulation development, clinical planning, and operations.
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Develop and lead all CMC-related activities including process chemistry, drug substance, drug product, analytical, supply chain, quality and formulation from lead optimization phase through to clinical development and commercialization.
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Serna Bio is a preclinical drug discovery company developing small molecules that can modulate translation and splicing, by targeting RNA. Founded in 2021, Serna Bio leverages the convergence of synthetic biology, machine learning (ML), and massively multiplex screening to tackle the historical challenges of drugging the RNA universe.
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Generate:Biomedicines is seeking an innovative and experienced visionary Senior Vice President, Drug Design and Preclinical Development to lead and revolutionize the development of new medicines using Generate:Biomedicines’ cutting edge platform.
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Significant global drug safety/pharmacovigilance experience, including experience in developing systems and processes for handling, processing, analysis, and regulatory reporting of adverse event reports, including serious adverse events.
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In collaboration with key stakeholders, identify, assess, prioritize, and pursue potential drug candidates through cell assays, animal and toxicology studies, and early human safety, biomarker and POC studies.
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The Vice President, Global Medical Safety will be responsible for providing medical oversight for the global drug safety and pharmacovigilance function to ensure proactive and timely benefit-risk assessments of all safety data.
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drug job Title: president in Cambridge, MA
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