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This position will serve as the Manager for the Clinical Trials Unit, directed by Dr. Ian Grant, and housed within the Mesulam Center for Cognitive Neurology and Alzheimer's Disease.
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Preferred: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) is preferred. Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification, along with a minimum of two years additional professional experience, will be considered in place of degree.
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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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As the primary resource for the protocols, the Clinical Research Coordinator will act as liaison between the investigators, primary care providers, the institutional review board (IRB), and the sponsor.
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Responsibilities Clinical Trials Operations – Overall Management Meet regularly with CRMs and ACRMs to review ongoing clinical trials activities: day to day protocol conduct execution adherence and to serve as the point person to resolve real time issues / conflicts that may prevent protocol conduct execution and or compliance.
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The CRU Regulatory Affairs Office seeks a full-time Regulatory Affairs Veeva Quality Assurance Specialist to participate in the review and migration of Phase I-V clinical trial investigator site files to the Veeva SiteVault platform.
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In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies for feasibility and evaluates potential competition with other protocols prior to submitting study.
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Active Kentucky Registered Nurse License or compact license with privileges to work in Kentucky (preferred) Or Current Licensed Clinical Social Worker (LCSW), Licensed Professional Clinical Counselor (LPCC), Licensed Marriage and Family Therapist (LMFT) or Licensed Psychological Associate (LPA) in the state of Kentucky (preferred.
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Clinical Research Coordinator C (CRC-C): In addition to above, the CRC-C will have limited supervision from the project manager and will need to use more independent judgment when managing their assigned clinical trials.
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Support IT Compliance during the following review meetings: Security Review Board (SRB) Meetings for Clinical Trials implications Architecture Review Board (ARB) Meetings for Clinical Trials implications Change Review Board meetings (CAB) Q-Suite Change Control and Release Lock meetings Quality Improvement Forum Safety Committee Team member for IT Business Continuity Periodic Management Review Meeting.
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Description Donor Review Coordinator Location: (Sabre)Virginia Beach, Virginia *This is not a remote position* Department: Quality Assurance Job Type: Full-Time Shift: Day shift; Monday-Friday, hours may varyClinical Classification: Non-Clinical LifeNet Health is searching for talented individuals who will embrace our mission of saving lives, restoring health, and giving hope.
$19.97 - $26.62 an hourFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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In addition to the responsibilities above, the Clinical Research Coordinator B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board (IRB) documentation through the IRB, including submissions, continuing reviews, amendments, modifications, and adverse event reporting.
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Reporting to the QRN Manager and under the guidance of SFHP Medical Director, the QRN will support and manage the review and resolution of Potential Quality Issues (PQIs) and other clinical quality related initiatives.
$52.56 - $64.25 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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HHC is also an active member of the Alliance for Clinical Trials in Oncology and NRG Oncology and has access to clinical trials offered by these groups. The ideal candidate would work closely with the Director of Neuro-Oncology, Alexis Demopoulos, to develop and deliver advanced treatment options through clinical research while providing comprehensive, coordinated, and outstanding clinical care for patients suffering from primary and secondary central nervous system neoplasms as well as the neurologic complications of cancer.
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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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review clinical trials jobs Title: manager clinical Company: Cpc Clinical Research
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