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Translational Medicine at our Research & Development Division is responsible for planning and management of an important inflection point in the drug development process, working closely with scientific, regulatory, statistical, and modelling colleagues across the organization to translate the benchtop science of preclinical discovery into compounds ready for assessment in large clinical populations.
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MD (nephrologist preferred) in a drug development-related discipline with 11+ years of experience in the pharmaceutical or biotechnology industry, with direct experience in drug development and 5+ years of leadership experience.
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Who You Are You are a seasoned leader with in-depth experience in drug development, supply chain or manufacturing. Advanced degree (MS, PhD, MBA) preferred in a relevant biopharmaceutical discipline Track record of effective matrix leadership experience in the setting of program teams across the full product life cycle, e.g., (CMC) PO&T line functions sub-teams or other cross-functional teams operating in a matrix environment ideally across an organization Experience with CMC, supply chain, or LCM development extending from IND to NDA/BLA, including a solid understanding of global registration processes.
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Enthusiastic about working in a drug discovery and development centric scientific environment. The Data Scientist will also interact with lab members emulating clinical trials in electronic health records using federated learning of target trial emulation with collaborators conducting molecular dynamic simulation for drug discovery, and with medicinal chemists conducting in silico screening.
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Prepare formulations and perform characterization assays/data analysis with focus on in vivo studies, drug carrier design/development, assay development etc. - Support vaccine formulation development activities.
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By combining leading-edge chemical sensing technology with exclusive methods of protein synthesis and stabilization, Kinovi will deliver to drug hunters what they have been asking for: drug-protein binding kinetics for every stage of the drug discovery process.
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Extensive understanding of drug development process and good understanding of commercial, legal, tax/finance and IP matters. Responsibilities include working with the Global Rare Disease Business Unit to identify prioritize and assess new Business Development opportunities, establish and nurture external relations, and lead negotiations with the counterparts across the different phases of the Business Development Processin alignment with the VP, Head of Global Business Development RARE.
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Dr. Iafrate’s laboratory is focused on precision oncology, including genetic and protein biomarker development utilizing NGS and mass spectrometry as well as traditional pathology methods. His laboratory is also developing novel therapeutics, utilizing CRISPR screens and high-content drug screens.
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Required: Experience in cancer biology, working in oncology drug discovery project teams, cancer cell-based assay design, assay development and drug testing. Contribute to target selection and target validation to ensure the development of a robust preclinical pipeline of valuable drug discovery programs.
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In this role, you will establish a highly functional group that supports drug discovery projects with assay development, structural enablement and general biochemistry needs. The Dana-Farber Cancer Institute seeks a scientist with experience in biochemistry, structural biology and assay development to lead the molecular sciences group at the newly established center for therapeutic discovery.
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Sr./Exec Director of Business Development Computation is revolutionizing drug discovery. 7-10 years in early drug discovery and development process. 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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Deep knowledge in pharmaceutical development: drug development, process chemistry, biologics, formulation development, analytical development, and/or statistics. Experienced leader in drug development of commercially viable product across modality and therapeutic areas.
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The Vice President of Global Drug Safety and Pharmacovigilance is a safety physician and a key leader in the Global Development Organization. Expert knowledge of domestic and international regulatory safety reporting requirements for investigational and marketed products, including FDA/ICH guidelines related to pharmacovigilance (e.g., E2B) and Good Clinical Practices, as well as a working knowledge of the Code of Federal Regulations regarding drug safety.
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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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Work with Preclinical Discovery BD group to continue servicing pre-existing clients into late stage API manufacturing and development. Responsible for driving sales of their API Drug Product services to biotech and pharmaceutical companies in the United States.
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drug development jobs in Waltham, MA
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