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Monitor competitive publications and technologies to stay abreast of developments in the field and to inform product development, preclinical, and clinical research. Our incredibly talented team of engineers, innovators, and industry leaders bring years of experience from the top healthcare companies in the world, including: Intuitive, Auris, Stryker, Johnson & Johnson, Boston Scientific, Verb Surgical, Mako, Think Surgical, Medrobotics, and Hansen.
$160,400 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Division of Pulmonary, Allergy, and Critical Care Medicine (PACCM) at Stanford University is one of the largest divisions in the Department of Medicine based on the number of faculty and the revenue generated by the division from clinical and research activity.
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Reporting to the Gynecologic Oncology Clinical Research Manager, the Clinical Research Coordinator 2- will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge.to conduct industry sponsored trials, cooperative group trials, investigator initiated clinical research studies, from start up to close out.
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The Sr. Director Drug Development Program Manager is a critical role within ReCode's PMO. PMO is responsible for delivering cross functional project management excellent to programs across the drug development lifecycle (Research, CMC, Pre-clinical and Clinical Development.
$200,000 a yearExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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8 + years of experience in clinical research, with a strong background in TMF management. The Manager of Trial Master File (TMF) Operations is responsible for the overall management, quality, and compliance of the TMF in accordance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and company policies.
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We research, develop, and commercialize innovative digital health products and solutions by bringing together the full capabilities of our team, including product strategy and management, clinical expertise, partnerships, UI/UX design, usability research, clinical research and validation, software development, AI / Gen AI, and regulatory submissions.
$251,950 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices.
$92,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The Clinical PK Manager will be a key part of the Clinical Pharmacology team responsible for Bioanalytical Contract Research Organization (CRO) oversight and represent the Clinical Pharmacology function at clinical study execution teams.
$158,000 a yearFull-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Zymeworks is looking for an experienced Senior Program Manager for our Early-Stage Clinical Development team, who is an industry-experienced professional with biologics experience, big-picture vision, ability to anticipate & facilitate cross-functional activities & decisions, ability to apply procedural solutions to research operations, attention to detail, and a drive for success.
$213,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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We require a motivated individual with a scientific background to play a critical role as a Procurement Manager within our Research and Development team. 5+ years of professional work experience plus a BS/BA; 3+ years of professional work experience plus an MA/MS or MBA in a corporate environment, preferably in procurement and supplier management.
$85 an hourFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Ph. D. in biomedical research (preferably in neurosciences) including 4+ years of post-PhD experience in project management, in industry. As a Project Manager, you will play a critical role in orchestrating cross-functional teams at the intersection of basic research discovery and drug development, managing project timelines, budgets, and resources, and ensuring the delivery of high-quality results.
Full-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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The Clinical Program Manager is responsible for managing the overall operation of pre-clinical and clinical trials including project planning, budget, resource management and, if required, contract research organization management (CRO.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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At least 5-6 years of clinical trial management experience in a Biotech, Pharmaceutical company, or Clinical Research Organization. Participates in assigned activities related to user acceptance testing (UAT) of clinical systems, including EDC and interactive response technology (IRT) and may contribute to the authoring of systems requirements.
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6+ years of clinical research experience, with at least 2 years' experience in planning and managing clinical trials. Understanding of clinical trial processes and experience in driving execution, from study start-up through study closure, (e.g., data management, safety, biostatistics, medical writing.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Previous experience implementing, helping and managing medical device trials Significant knowledge of clinical and/or outcomes research study design. Minimum Advanced degree in a scientific/bioengineering field (M.S., Ph. D. or M.D.) with a minimum of 5 years of experience in clinical research, or Bachelor’s degree in a scientific/bioengineering field with a minimum of 8 years of experience in clinical research is preferred, or a minimum of 10 years of experience in clinical research with relevant training.
$200,600 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago
experience manager clinical research jobs in Stanford, CA
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