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The Associate Principal Scientist will work closely with individuals from PaCES, Clinical Research, Regulatory Affairs, Biostatistics, Outcomes Research, and Operations to ensure COA endpoint strategies are consistent with and correctly executed to support the product strategy.
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Two years of experience working as a clinical laboratory scientist (CLS) in a medical laboratory preferred. California Clinical Laboratory Scientist (CLS) License required. The position is a clinical license position and a journey level classification in the Clinical Lab Scientist classification series.
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Incyte Corporation is seeking a motivated and experienced protein purification scientist to provide technical expertise in monoclonal antibody (including bispecifics) purification process development, characterization, and validation primarily for novel therapeutic monoclonal antibody products throughout all stages of clinical trials and commercialization.
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Provide regulatory guidance to PI's and Research Staff to support the successful submission of regulatory compliant materials that are approved by the IRB or IACUC as applicable. Assist the Research Quality Improvement Specialist in monitoring of BRI-sponsored clinical research according to Federal Guidelines and Good Clinical Practice (GCP) by participating in the monitoring visits for verification.
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The department of Computational Biology is seeking an experienced lead or principal-level bioinformatics research scientist to provide direction and lead the development of pipelines for use in our clinical genomics program.
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The oncology clinical research nurse I is expected to develop and maintain competencies in clinical research nursing in the first year of the position including but not limited to comprehension and compliance with all NYU PCC Clinical Trials Office policies and procedures, NYU OSR and IRB policies and procedures, familiarity and application of Good Clinical Practice (GCP) guidelines and Federal Regulations that govern the conduct of human subjects research.
$100,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As a Clinical Research Coordinator I, you will work independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
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Clinical Research Nurse serves as an expert oncology clinician and patient/client advocate. The Clinical Research Nurse assists the Principal Investigators (PI’s) and other participating physicians and investigators in the initial identification and evaluation of protocols to be submitted to IRB/CIRB for approval.
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Position Summary Reporting directly to the Executive Director of the Clinical Trials Office (CTO), the Associate Director for Operations (Associate Director) is responsible for the management and oversight of business operations and finance in the CTO at the Vagelos College of Physicians and Surgeons (VP&S) and NewYork-Presbyterian Hospital (NYPH.
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5% Initiates and maintains clinical research regulatory compliance for assigned protocols including but not limited to the IRB approval and regulatory documents per FDA, HHS and GCP guidelines.
$87,500 a yearPart-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The successful candidate will be expected to work in a team environment, to test computational physics models in large production software, publish the research in peer-reviewed journals, and present work at international conferences.
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Our clinical operations activities are growing rapidly, and Medpace currently has multiple full-time leadership openings within our Clinical Operations team ranging from Site Payments Manager I through Associate Director, Site Payments.
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Under the direction of the Director of Accreditation, Cancer Registry and Clinical Research, identify, abstract and maintain records for all eligible cases of malignancy, adhering to American College of Surgeons (ACoS) and UM BWMC Oncology Registry standards and procedures.
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To provide clinical and surgical medical care of animals (multi-species) used in research and training. Provides clinical and surgical medical care to research animals. To participate in all activities that are part of a dynamic laboratory animal care and use program including research, grant writing, equipment and process evaluation, tours and the development of standard operating procedures.
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Provides study start-up documents (paper or electronic) to Clinical Research Regulatory Coordinator. Supports the Clinical Research Regulatory Coordinator in the maintenance of regulatory documents in accordance with SOPs. Develops accurate source materials and ensures compliance from study team.
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clinical research regulatory associate jobs Company: Novo Nordisk A S in TX, Us
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