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Four-time Forbes Magazine's Best Places to Work in America , is seeking a Scrum Master to join our growing Agile development team. Scrum Master - Enhance Lives & Drive Innovation at a Ecommerce Leader (Mobile & Enterprise Web.
RemoteExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Clinical Operations plays a key role in ensuring all Client clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of Gilead’s products.
$64 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Review and oversee study plans, including Clinical Monitoring, Communication, Project Management, and electronic Trial Master File (eTMF) Management. Solid understanding of the Trial Master File (TMF) structure, particularly the DIA model.
ExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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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 Workspace tools (email, calendar, docs, sheets, slides, etc.
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The Director/Sr. Director, Trial Master File (TMF) Operations is accountable for the leadership of the TMF organization, inclusive of TMF technology & systems, TMF operations, and TMF inspection readiness.
$260,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Ensure the required study-specific CDS documents in the Trial Master File (TMF) are of high quality and are filed contemporaneously. Serve as Clinical Data Scientist and Trial Lead for one or more clinical trials assuming responsibility for all CDS activities including selection and application of data acquisition standards, Data Management Plan, selection of quality risk indicators, third party study data due diligence.
$155,900 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Numerous innovative research programs available including the only Mobile Stroke Unit (MSU) in Northern California, Sutter-wide Research Institute and IRB providing support for participation in clinical trials.
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Additionally, the Clinical Procurement Coordinator supports donor families, provides family care and may provide families with the option of organ and/or tissue donation. GENERAL JOB FUNCTION The Clinical Procurement Coordinator is responsible for response to donor referrals, donor evaluation, and donor management, coordination of organ recovery, organ preservation, and organ distribution.
$42.66 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Leads and/or participates in the development and review of study documents including CRF design, project plans, Service Provider Oversight plans, TMF (Trial Master File) plan. The Sr. CTM will be responsible for the day-to-day oversight of global clinical trials and will manage internal stakeholders, CROs, multiple service providers, clinical monitors, and clinical trial sites.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Client clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of client's products.
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Responsible for filing necessary documents in the electronic trial master file (eTMF), and supporting regular cross-functional reviews of the eTMF.Assist in the creation of training slides and lead training sessions for CRO or investigative sites.
$114,500 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Licensed Master Social Worker (LMSW) Licensed Clinical Social Worker (LCSW) Licensed Clinical Social Worker Psychotherapy (LCSW-R) Licensed Professional Clinical Counselor (LPCC.
$70,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Community Practice Clinical Data Coordinator at Trial Library will play an integral part in expanding access to cancer clinical trials by pioneering pre-screening efforts in community oncology settings.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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We seek a geriatrician who is a national leader and mentor in geriatrics and gerontology and is a candidate for appointment as Associate Professor or Full Professor in the In Residence (Research) series in the Division of Geriatrics, Department of Medicine, UCSF. Candidates should be ABIM certified in Geriatric Medicine and have demonstrated competence in the practice and teaching of clinical geriatrics.
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This position requires expertise in various aspects of patent litigation, including trial preparation, motions, depositions, and discovery management. Experience with Patent Trial and Appeal Board (PTAB) and International Trade Commission (ITC) proceedings is a plus.
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clinical trials trial master file jobs Title: trial master file in South San Francisco, CA
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