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Plan, develop, and execute relevant bench-top, pre-clinical and cadaver studies as needed for regulatory, clinical and R&D requirements. About the Role : The Sr. Research and Development Engineer will be helping to advance the company’s minimally invasive low back pain technology, Intracept.
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In depth knowledge of regulatory requirements in working with research animals, experience in laboratory animal medicine and science, animal husbandry and vivarium operations. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world.
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The Pediatric Cardiology Service Line Administrator works in partnership with the Chiefs of Pediatric Cardiology and Pediatric Cardiothoracic Surgery, and the VP Operations, CHoR to manage the financial and non-clinical oversight of the programmatic and non-clinical operations for the service line (e.g., pediatric cardiology, pediatric non-invasive cardiology imaging, pediatric heart station, and the pediatric cardiac catheterization and electrophysiology lab, etc.
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Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it.
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Position oversees and coordinates complex clinical research studies; serves as a resource to provide comprehensive information to clinical research staff by promoting a smooth operation of clinical research; responsible for preparation of budgetary reports and ensures billing and regulatory compliance standards are maintained; may supervise clinical research staff.
$66,700 - $103,400 a yearExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The Office of Laboratory Animal Care (OLAC) Director and University Attending Veterinarian (UAV) has responsibility for all animals used in research and teaching at the University of Tennessee Knoxville, a land-grant university.
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As needed, project management of Clinical Research Organizations (CRO) conducting post-market follow-up (PMCF) clinical studies when CooperVision is considered the SponsorTravel up to 10.
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Prepares clinical study documents and coordinates with additional collaborators including product management, statistician, regulatory affairs, clinical research management, and contract research organizations (CROs.
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The Clinical Lab Assistant reflects the mission, vision, and values of NM, adheres to the organization's Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards.
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As Deputy Chief, the incumbent will work closely with the Section Chief to ensure that the highest standards of clinical care are adequately reflected in standardized assessments of performance and regulatory compliance.
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Experience as a Clinical Research Associate or Clinical Research Coordinator required. Manage and/or support global clinical trials (Phase 1-3) in oncology indications, ensuring that studies are carried out in accordance with the clinical development plan, ICH-GCP, and FDA/other regulatory agency requirements.
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The laboratories of A.M. Barrett and Kevin Houston are seeking an experienced clinical research coordinator who is knowledgeable about regulatory guidelines and comfortable managing small to medium-sized clinical trials.
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2 yrs clinical/research experience in Organ/Tissue Recovery, Hospital, or govt. Reviews and recommends policies and procedures to ensure clinical practice compliance in organ/tissue donation and recovery and identifies the need for new policy developments or policy changes to meet regulatory requirements.
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Medical expert responsible for the development of clinical research strategies and independent direction of Phase 1-3 clinical studies while working with cross-functional project teams (clinical project managers, research, preclinical/clinical pharmacology, biometrics, regulatory, drug safety, CMC), creation and execution of clinical development plans, and the development of strategies that will ultimately lead to approvals of Neurocrine's products.
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Position Summary: The Clinical Research Coordinator III, as a certified research professional, handles clinical trial administration for all protocol phases for the Leukemia and Lymphoma Disease department.
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