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Trial Master File Records Specialist (TRS) Responsibilities. The TRS will provide services onsite (hybrid position) at our Ridgefield, CT location supporting our Trial Master File (TMF) team.
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Serve as the subject matter expert on Veeva Vault and related clinical trial management systems (CTMS), electronic trial master file (eTMF), and regulatory document management systems.
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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.
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Manage and provide oversight to the CDM section of the Trial Master File. Reporting to the Executive Director, CDM, the Senior Manager, CDM will be a highly motivated, quality-focused individual who can work collaboratively in a fast-paced, cross-functional team environment, and will oversee data management activities across multiple studies from study start-up through study closure in support of clinical trial objectives and corporate goals.
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The Administrative Director of Cancer Clinical Trials serves as operational lead of UMMC's Cancer Center and Research Institute (CCRI) clinical trial and clinical research program.
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The UCSF Department of Surgery is recruiting for a Clinical Research Nurse to manage several clinical trials in the Division of Transplant, with a primary focus on islet transplantation for treatment of diabetes.
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Ensures study compliance with OPUS SOPs and regulatory guidelines by performing periodic quality control audits of any trial master file (TMF) maintained by the Service Provider (SP) before study initiation, during and at the end of a study.
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Court Interpreter 2- Master - The salary range for this position is $73,674.60 to $111,206.94 for Schedule A, and $73,674.60 to $105,646.59 for Schedule B. Employees at this level may interpret complex legal proceedings; translate forms, letters and other court-related documents; mentor Court Interpreters; and interpret for trials that are high profile, complex, and which involving crimes of the first degree.
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This position is housed in the Clinical Research Support Office (CRSO), a centralized clinical trial management office in the UCSF Helen Diller Family Comprehensive Cancer Center (HDFCCC), which provides project management and clinical research coordinator staff, and regulatory services for oncology related clinical trials.
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Review and file necessary vendor laboratory documents for the Trial Master File (TMF) as applicable. Advanced understanding of clinical trial processes from study start-up through study closure related to sample collection, logistics, transit, storage, central tracking and global requirements.
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Higher salary is negotiable with candidates who have experience with Psychometrician / Psychological Rater experience in pharmaceutical clinical trials. Healthy Brain Clinic, a research site specializing in clinical trials of Alzheimer's Disease, is seeking applicants for a Clinical Scientist (Psychological Rater.
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Our department is responsible for defining and executing biomarker strategies in our clinical trials, and using human clinical translational research to generate novel target and biomarker approaches in MS. Through our clinical trials, as well as our translational research efforts, our group identifies new targets and implements biomarkers to evaluate disease heterogeneity, target engagement, mechanism of action, and disease modification.
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A Clinical Research Coordinator I is asked to perform an increasing complexity of tasks to facilitate clinical trials at Virginia Mason, working with a variety of sponsors ranging from large pharma and biotech sponsors to small non-profit grant awards.
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Oversee completeness of data management documentation for the Trial Master File. The Senior Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up to post database lock for assigned projects.
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This position will support Quality Control clinical testing activities for cell and gene therapy clinical trials to treat patients with cancer and HIV supported by the Clinical Cell and Vaccine Production Facility (CVPF) at the University of Pennsylvania.
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clinical trials trial master file jobs Title: trial master file
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