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SUMMARY/JOB PURPOSE: The Senior Staff Engineer, Product Management - Business Applications will ensure high-quality Drug Development Business Applications support. The role will lead the delivery of Support, DevOps, and initiatives in Global Patient Safety (GPS) functions from a Drug Development perspective.
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The role collaborates closely with Drug Safety Operations staff (on medical aspects of ICSRs) and Clinical Development (medical ICSR discussion and follow-up, as well as safety surveillance.
$200Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Eikon's discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.
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Nine years of drug development experience in biotechnology or pharmaceutical industry, or a combination of academia and industry. In collaboration with the Exelixis clinical teams, the primary role is to lead and execute early-stage clinical trials for oncology products in development.
$304,500 - $432,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Scientist IV, Bioconjugation (ADC) Process Development, will have an opportunity to contribute to Exelixis' Antibody Drug Conjugates (ADCs) technology platforms. The successful candidate will be responsible for the development of scale-able and robust downstream ADC processes and support technology transfer efforts, leading to clinical GMP manufacturing of ADCs.
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We are passionate about all the ways our technology can impact R&D and industrial applications including microbial characterization and identification, synthetic biology, biomanufacturing, bioprocess development, metabolic and mitochondrial disorders, nutrition, toxicology, and drug discovery.
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Working knowledge of the drug discovery and development process and ability to understand risks and requirements associated with pharmaceutical contracting preferred. Ability to work effectively across a variety of functional groups such as Commercial, Research and Development, Chemistry Manufacturing Controls (CMC), Clinical Studies and Finance,) and all levels of management.
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Thorough understanding of the drug development process and context applicable to safety surveillance activities. Provide safety science and pharmacovigilance subject matter expertise on program and study teams as well as other cross-functional platforms throughout the company.
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Degree in Pharmacy, Nursing, Epidemiology, Biosciences or equivalent healthcare degree with pharmaceutical industry background and proven competence in PV. Solid foundation in GCP and GVP regulations. Review and synthesis of individual case reports as well as aggregate data summaries.
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Working knowledge of the drug discovery and development process and ability to understand. and Development, Chemistry Manufacturing Controls (CMC), Clinical Studies and Finance,) and all.
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Minimum 10+ years of relevant experience in drug development or quality system in a biopharmaceutical industry, with a minimum of 3 years of project management or functional team lead experience required.
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Detailed knowledge of clinical trial implementation and drug development process. Three to Five years of clinical development experience in the biotechnology or pharmaceutical industry or a combination of academia and industry.
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Expertise in liquid handler method development on platforms like HamiltonSTAR or Vantage, Tecan Fluent or Evo, Bravo, and EL406 plate washers. Expertise in liquid handler method development on platforms like HamiltonSTAR or Vantage, Tecan Fluent or Evo, Bravo, and EL406 plate washers.
$125,000 - $136,800 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Ph. D.in life science field or MD degree, with 7-10 years of experience in drug development, pharma translational research, biomarker and diagnostics experience; or a MS/MBA in relevant life sciences field with 10 years experience in pharma research and development.
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Position requires a Bachelor’s degree, or foreign degree equivalent, in Computer Science or “STEM” Majors (Science, Technology, Engineering and Math), and 6 years of progressively responsible post-Bachelor’s degree experience in a related software development occupation.
$179,520 - $269,280 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago
drug development jobs in Hayward, CA
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