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This includes partnering with PMed Biomarker Leads and being responsible for editing clinical documents, sample management, data management, cross-functional teams, budget management and strategy documents.
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There is an exciting opportunity within the Precision Medicine Oncology Biomarker Program Management (BPM) group at AbbVie. The Precision Medicine group uses advanced methods to discover biomarkers for use in clinical trials.
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Work with bioanalytical team members on activities related to assay development, sample management, pharmacogenomics and biomarker development. Travel %Educational QualificationsPhD, PharmD, MS in Clinical Pharmacology (or a related area such as pharmacokinetics, pharmacology, pharmaceutics) with a minimum of 5 years of experience in these areas.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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There is an exciting opportunity within the Precision Medicine Biomarker Program Management (BPM) group at AbbVie. The Precision Medicine group uses advanced methods to discover biomarkers for use in clinical trials.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Good documentation practices, laboratory safety policies, Quality Management System policies, RNA/ DNA extraction, LIMS, Medical terminology, sample accessioning, sample testing, reporting.
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This position manages the day-to-day operation of the core instruments (HPLC and mass spectrometry), and works with clinical and biomedical researchers with different disciplines, including proteomic experimental design and sample preparation for proteomic analyses.
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As a Junior Clinical Research Coordinator, you are responsible for assisting with the management and coordination of all aspects of conducting clinical trials within s RII, surgery centers, both clinically and administrative/regulatory.
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Facilitating sample management and movement: coordinating the management and movement of samples for biomarker research projects, ensuring compliance with relevant regulations and guidelines.
$122,800 - $193,300 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Sample management and sample data QC in LIMS. The main responsibilities of a Biologist II involve pre-clinical sample analysis using a ligand binding assay. Sample and reagent management using electronic tools such as Laboratory Information Management System (rLIMS) and others.
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Participate in sample management activities such as receiving, processing, storage, and shipping pre-clinical samples. + Collaborate in laboratory management activities such as receiving, tracking, storage, and maintenance of laboratory reagent stock.
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Draft/revise SOPs and work instructions for sample management activities. " Prior biological sample management experience, is a plus. " Support sample management for routine in-process testing.
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Oversees set-up and maintenance of study systems which may include Clinical Trial Management System (CTMS), Trial Master File (TMF), study SharePoint etc. Assigns tasks to Clinical Study Management staff and supports their deliverables.
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Proclinical is seeking a Stability Sample Management Specialist for a leading pharmaceutical company. This role is responsible for all aspects of on-site stability sample storage and sample management.
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The RA will perform sample accessioning, aliquoting, perform assays, report results, maintain inventory and quality management for the CDS. Key areas of responsibilities include conducting clinical and research activities/experiments, collecting, analyzing, and summarizing data, preparing reports, contributing to manuscripts/publications, administrative and project management, facilities and equipment management, and supervision/staffing.
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The Statistical Analyst will also assist with designing interfaces for data collection and management, performing data integration, manuscript writing for peer reviewed medical journals, including generating figures and tables, and will support grant development with sample size calculations.
ExpandApply NowActive JobUpdated 4 days ago
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