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Ensure that all programming and data are conducted in compliance with GCP, relevant SOPs, and regulatory requirements; review and file study documentation in the trial master file (TMF) system acceptable for audit.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Working within a team environment and leading functional internal audits of VO's electronical Trial Master File (eTMF) and Contract Repositories to ensure meticulous oversight of VO's documentations, adherence to work procedures, compliance standards, and the preservation of data integrity.
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Proficiency in (or willingness to learn) instructional and other technology, such as: Learning Management Systems (Canvas); lecture/presentation capture applications (Panopto); online video conferencing (Zoom); Microsoft Office (Word and PowerPoint); file sharing (Google drive or Dropbox); and Google tools (email, calendar, docs, sheets, slides, etc.
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Daily activities will include, but are not limited to, working within a team environment and leading functional internal audits of VOs electronical Trial Master File (eTMF) and Contract Repositories to ensure meticulous oversight of VOs documentations, adherence to work procedures, compliance standards, and the preservation of data integrity.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Understand & perform SAP CRM & hybris configuration including Customer/User master data, Catalog Management, Content Management, Workflows, Promotions/Vouchers, Shopping Cart & checkout, Search and guided navigation, Returns Management, Payments, Customer specific Pricing, Sync & Async Order Mgmt with SAP etc.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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It does not refer to the “Master of Fine Arts” (MFA) degree when that degree is based on specialization in performing arts or dance, film, video, photography, creative writing, or other nonplastic arts.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Expert in digital media technology and editing software packages (familiarity with file formats, codecs, and color spaces, along with Adobe Creative Suite, specifically Premiere Pro, After Effects, and Illustrator.
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The Sr. Clinical Trial Manager/Clinical Trial Manager, Clinical Operations (Sr. CTM/CTM) will report to the Associate Director, Clinical Operations and will be responsible for assisting in the oversight and management of clinical trial execution.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Thorough understanding of clinical trial reporting process, as well as regulatory reporting requirements including electronic data submissions and CDISC implementation. Conduct hands-on validation/QC of CRO deliverables to ensure high-quality (SDTMs, ADaMs, TFLs) and ensure accuracy of clinical trial results for internal and external audiences.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Review study plans, including; Clinical Monitoring, Communication, Project Management, and electronic Trial Master File (eTMF) Management. Strong understanding of the Trial Master File structure (TMF.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Minimum Requirements: Currently has, or is in the process of obtaining a PhD or Master degree in Computer Science or a related STEM field Solid foundation in 3D math, linear algebra, computational geometry and numerical analysisDeep understanding of and experience with the latest deep learning techniques related to NLP, computer graphics and multi-modal systems.
InternExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The Sr. Research Associate will support the Discovery Bioscience team and assist in developing and executing screening assays for the evaluation of AAV vector products. Senior Research Associate, Discovery Bioscience.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Works collaboratively with vendors, Clinical Research, Drug Safety, Regulatory Affairs, Clinical Operation, and Project Management teams to meet project deliverables and timelines for statistical data analysis and reporting.
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Oversee assigned studies through review of monitoring visit reports and Trial Master File QC reports. The Clinical Trial Manager is responsible for managing the day-to-day operations of assigned clinical studies to ensure completion per established project team goals and objectives.
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DescriptionThe research group of Dr. Elaine Yu at Vitalant Research Institute (VRI), an affiliate of the University of California, San Francisco (UCSF), is seeking talented and highly motivated Research Associate I. The Research Associate will focus on statistical and bioinformatic analyses for several studies regarding cardiometabolic health among blood donors.
$64,500 - $70,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago
trial master file jobs Title: clinical research associate Company: Parexel in South San Francisco, CA
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