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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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Guides and ensures that the clinical study documentation (documents, images and other digital content) is correctly filed and archived, and that the study is maintained in a trial master file (TMF), so that documentation of GCP compliance is available, if required by a regulatory agency.
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Manage site regulatory documents and Trial Master File (TMF) The Coordinating Center Senior Project Manager for the Center for Clinical Investigation Coordinating Center (CCI-CC) will report to and work closely with the CCI-CC Director in the development, implementation, and management of the clinical trial operations for ongoing clinical trials and research consortiums.
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The research nuclear medicine technologist (RNMT), working under the general supervision of the study Principal Investigator and the Research project Manager provides coordination for designated clinical trial activities in Nuclear Cardiology.
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Ideally, minimum of 2 years working within an academic clinical trial coordinating center. Site activation, training, and trial conduct. Manage study portal and access to study documents and trial material.
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GENERAL SUMMARY/ OVERVIEW STATEMENT: This department of psychiatry, Massachusetts General Hospital, Harvard Medical School is hiring a full time or part time coordinator for a National Institute of Health (NIH) funded multi-year clinical trial of young (18 – 24 yrs.
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The Senior Clinical Trial Manager will play a crucial role in overseeing and managing Phase 1-3 clinical trials related pertaining to mRNA therapies targeting cancer and rare disease.
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Scope of ResponsibilityWill serve as a key strategic partner representing Global CMC Regulatory on Regulatory Networks and Matrix Teams, providing and overseeing strategic direction and guidance to Biopharmaceutical and/or CGT R&D, Pharma Supply Chain, Clinical Trial Supply, Quality Assurance, and Commercial interfaces on both global project and key strategic business initiatives.
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Sanofi is recruiting a new Global medical Director to support post- regulatory authorization clinical trial program for dupilumab in the Global respiratory Franchise for the respiratory indications including asthma and Chronic Obstructive Pulmonary Disease (COPD) for dupilumab and itep.
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Working knowledge of the fiscal policies of the Trial Court and ability to prepare fiscal reports. The Trial Court is a qualifying employer for Federal Student Loan forgiveness To learn more about this program, and all of our benefits, click here.
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Job Overview: Seeking a Clinical Research Scientist with strong expertise in Oncology, Immunology, or Immuno-oncology to lead the implementation, planning, and execution of clinical trial activities, collaborating with various stakeholders and driving Clinical Development strategy in a fast-paced, collaborative environment.
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OverviewThe Tufts University School of Medicine’s Graduate Programs’ Department confers the Doctorate in Physical Therapy (DPT), Master of Public Health (MPH), Master of Medical Science (MMS) by the Physician Assistant Program, Master of Science in Health Informatics and Analytics (MS-HIA), and Master of Science in Biomedical Sciences (MBS.
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Master in Landscape Architecture (MLA) and Registration as a Licensed Landscape Architect (or in process) preferred. Works on the development of Neighborhood Plans, Master Plans and Zoning amendments.
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Reporting to the VP of Biometrics, the Director/Sr. Director, Clinical Data Management is responsible for all clinical data management activities related to the effective planning and timely delivery of complete, high quality and reliable clinical trial data.
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The Talend ETL Developer is a key member of CHIA’s software development organization and our Data Operations and Technology team reporting to the Associate Director of Master Data Management and ETL Design.
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trial master jobs Title: clinical research associate Company: Parexel in Waltham, MA
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