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You will work closely with Research, Clinical Development, Regulatory Affairs, and Program Teams to ensure seamless integration of translational activities into clinical trial protocols that are needed to address key biological questions about mechanism of action, identify patient populations most likely to benefit, evaluate therapeutic combinations, and generate novel biomarkers of response, and to ensure program execution.
$340,000 a yearFull-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Understanding of clinical research methods and operations, the Institutional Review Board, the Food and Drug Administration IND and IDE submission processes and submitted to other research review committees and regulatory bodies.
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You Have:3+ years direct experience with federal regulatory examinations (FDIC, FRB, OCC, or CFPB) and bank partnership lending models. You will work with partners in legal, operations, compliance, finance, data analytics and engineering, product and other teams, to ensure that Block is compliant with applicable requirements and obligations while, to the extent possible, streamlining regulatory impact and facilitating innovation.
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Experience with research-stage biophysical characterization for developability and/or basic assay development with in vitro cellular assays using cell lines or primary cells is preferred. HI-Bio, Inc., a Biogen company is seeking a highly motivated Senior Associate Scientist (SAS) with a background in antibody engineering to drive the discovery and validation of novel therapeutic targets in autoimmune and inflammatory diseases.
$97,500 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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In this function, the candidate will be translating pre-clinical /research methods and data to develop cGMP compliant processes and clinical drug product specifications, manage the execution of CMC studies and author drug substance/product IND sections.
$185,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The company is building out its pipeline of potential in vivo gene editing therapeutics and capabilities and has partnerships with leading pharmaceutical and biotechnology companies to broaden the reach of its innovative and proprietary technology.
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POSITION SUMMARY Reporting to the Managing Counsel, Health Affairs, Privacy & Data Protection Law, the Principal Counsel - Health Regulatory provides primary legal support to the University's medical centers and health sciences schools on complex and high impact healthcare regulatory analysis.
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This position is part of a faculty cluster hire to build UCSF Osher Center capacity in integrative health equity through innovative faculty who bring diverse backgrounds, research, and clinical expertise.
$377,200 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Following the Ph. D., 2+ years of mathematical modeling & computer simulation experience in the pharmaceutical industry for the Sr. Research Investigator level or 5+ years for the Associate Director level.
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Preferred Experience Proficiency in qualitative research methods (e.g., interviews, expert consultation, case studies). Our primary offerings include: Program Design and Strategy DevelopmentProgrammatic Research, Analysis, and ModelingGrant Support: Sourcing, Conducting Due Diligence, Making Grant Recommendations, Grantee ManagementProject Incubation, Nonprofit Business Planning, Organizational Development, and Staffing SupportEvaluation and LearningFacilitation, Collaboration, and Grantee ConveningRecruiting and Organization Design About the RoleCEA is looking for a Research Associate.
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Ardor Health Solutions is seeking a travel Clinical Lab Scientist (CLS) for a travel job in San Francisco, California. Specialty: Clinical Lab Scientist (CLS) Ardor Health Solutions is looking for a Clinical Laboratory Scientist to join our travel team in a Hospital setting, in San Francisco, CA.
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HI-Bio, Inc., a Biogen company, is seeking a Principal Clinical Scientist to support clinical research activities for our portfolio our immunology clinical programs, with a specific emphasis on severe immune-mediated diseases related to glomerular kidney disease.
$239,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Chief among the role's responsibilities involve full cycle examination management support including managing intake of examination requests, work with partners to obtain responses, facilitate regulatory submissions in the appropriate time frame and manage communications with partners.
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Conduct user research on the perception of privacy for Airbnb users. 4+ years experience in privacy, compliance, security operations and program management, preferably in a global B2C technology company.
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Connect with and gain access, establish long-term, strategic scientific relationships with KOLs, and connect KOLs to appropriate company partners ensuring research, scientific, and clinical interests are communicated.
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clinical research pharmaceutical company regulatory jobs Company: Wirb Copernicus Group in San Francisco, CA
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