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Lead the study start-up process, including, but not limited to, the Trial Kick-off meeting, the set-up of the trial master file (TMF), the set-up of the electronic data capturing (EDC) system, site selection, and the finalization of site Clinical Trial Agreements and budgets.
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The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs. Key Responsibilities In collaboration with other members of the clinical research site team works to ensure the execution of assigned studies.
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Our core practice areas include: clinical research; vaccine research, microbiology and infectious disease research, development and production; biodefense; global health security; and HIV/AIDS programs.
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Assist the PI and senior study team members in the management of study data for new and ongoing clinical research studies assigned. Clinical Research Coordinator ( 2 positions) School of Medicine, Internal Medicine/Pauley Heart CenterVirginia Commonwealth University (VCU) School of Medicine is a premier academic medical center located in the heart of Richmond.
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A Brief OverviewAbout the Department:The Clinical Research Coordinator I (CRC) will work in the Craig-Dalsimer Division of Adolescent Medicine at the Children’s Hospital of Philadelphia (CHOP) and PolicyLab in the Research Institute.
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Primary Duties and ResponsibilitiesThe Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study.
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Senior Clinical Research Specialist, Duke Cancer Institute Work Arrangement: Requisition Number: 245408 Regular or Temporary: Regular Location: Durham, NC, US, 27710 Personnel Area: MEDICAL CENTER Date: Jul 6, 2024 School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools.
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We are looking for a self-directed professional to support Digital Health Technology [DHT] (wearable sensors) and imaging components set-up and monitoring within clinical trials; specifically focused on the operational initiation/set-up, vendor and digital data/imaging monitoring, and data cleaning process efforts that occur within the Biomeasures Endpoints and Study Technologies (BEST) projects.
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As a 5-Axis Set-Up Machinist (also known as CNC Machinist, Journeyman Machinist), you will be responsible for setting up CNC machine tools, manufacturing and repairing parts, and ensuring quality control.
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The Research Nurse I is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. Preferred Qualifications⢠Bachelor of Science in Nursing strongly desired⢠Certification as a Certified Clinical Research Coordinator (CCRC through the Association of Clinical Research Professionals or ACRP) OR Certified Clinical Research Professional (CCRP through the Society of Clinical Research Associates or SoCRA) is strongly desired.
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Job Description ROLE SUMMARYThe purpose of the Senior Director of Clinical Research role is to coordinate and lead the development of first in man (FIH), proof of mechanism (POM), proof of clinical activity (SoCA) and proof of concept (PoC) and dose ranging studies for novel biological and small molecule therapies in Immunology, Inflammation and Neurology focused programs.
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The Clinical Trial Manager (CTM) is accountable for delivery of selected and/or regional deliverables within a trial (e.g., manage and oversee vendor deliverables, collaborate with functions to set up activities [e.g., Calyx, IRT, eRT], support site activation and recruitment, support data review/cleaning activities, support PI/ICF development.
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Assist the Clinical/Site Ops leads on the set-up/start-up of research site to prepare for start-up and conduct of clinical trials. The SiteBridge network extends reach further into these communities to empower a broader set of patients with some of the highest unmet needs to take part in clinical research to improve health outcomes.
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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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Certified Clinical Research Coordinator (CCRC) or other applicable certification preferred for IDC Research position. We are looking for a 1.0 FTE.Please visit our website for more information about our program: This research nurse position will work collaboratively with physicians in identifying and managing patients on NCI and pharmaceutical sponsored clinical trials.
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clinical research set up jobs Title: clinical senior research associate
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