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Clinical Research Coordinator for Large Neuroimaging Study of Aging and Alzheimer’s disease. These projects are related to the Stanford Aging and Memory Study (SAMS), an ongoing longitudinal imaging-biofluid study of healthy aging.
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Provides sample management expertise to the Study Management Teams (SMTs), Biomarker SubTeams (BSTs), and Clinical Pharmacology Subteams (CPST) Organizes and leads Biomarker and Bioanalytical operational meetings with study functional groups or vendors.
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Provides sample management expertise to the Study Management Teams, Biomarker SubTeams, and Clinical Pharmacology Subteams. Leads or otherwise assists in the preparation of interim and final study reports, including resolving any data discrepancies when biomarker data is needed for primary, secondary or support.
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Outsourcing, Clinical Operations, and Data Management) to ensure efficient execution of the study biomarker strategy. protocols and other study documents, contribute to process development and/or participate in special projects.
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Ability to manage any component of full cycle study management, from start-up to close-out. Provides input into study protocols and case report forms, authors informed consents, study plans, and presentations.
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Establishes strong cross-functional relationships and exhibits strong leadership skills with counterparts in other functional teams (e.g., Biomarker Sciences, Vendor Outsourcing, Clinical Operations, and Data Management) to ensure efficient execution of the study biomarker strategy.
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Provides sample management expertise to the Study Management Teams (SMTs), Biomarker SubTeams (BSTs), and Clinical Pharmacology Subteams (CPST) Accountable for ensuring biological samples collected are of good analyzable quality and are collected in adherence to the highest standards of ethics and informed consent.
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Strong understanding of science and drug development, with specific expertise in nonclinical study design, preclinical CROs, data management systems, nonclinical study procedures, and statistical analysis methods.
$265,000 - $300,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The successful candidate has experience in drug-development process, clinical study lifecycle, regulatory compliance, and the uses of real world evidence in clinical development and safety endeavors.
$221,170 - $286,220 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Oversee and provide strategic direction for Toxicology/Pathology, BioAnalytical/DMPK, Biomarkers, and Clinical Pharmacology teams to ensure robust support for clinical development programs. 12+ years of experience in the biopharma industry in non-clinical development (toxicology, pharmacology, pharmacokinetics, bioanalytical sciences, or related discipline.
$265,000 - $300,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Supports CTM and/or Study Director and cross-functional representatives as required in relationship management tasks (e.g. contracts, study logistics, patient enrollments, safety, data management, etc.
$121,000 - $160,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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You will assist in the review of clinical study protocols and other study documents, contribute to process development and/or participate in special projects. You will manage certain components of clinical studies and act as a member of the study team.
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The incumbent will serve as a liaison to high school and adult schools in developing non-credit career preparation, programs of study, academies, and bridge programs to facilitate the transition of secondary students into CTE programs at De Anza College.
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Shepherd our electrical ground support equipment through regulatory approval in the U.S. and abroad; examples include field listing or factory listing of power handling equipment. The position will play an active role in electrical code development as it relates to site safety for novel DC charging equipment with integrated aircraft thermal management, innovative battery energy storage systems, and other electrical infrastructure to support a first in class aircraft charging system development and deployment.
$91,400 - $140,900 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The Sr CM may assist with approvals of costs above study approved FMV. Order and maintain ancillary clinical study supplies required for conduct of clinical trials, including copying, printing study documents, reference binders, and arrange shipping, tracking, accordingly.
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