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The OCR Clinical Research Monitor II, completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial research both from a documentation and process level.
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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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The CRC B (Regulatory Coordinator) will assist with preparing and processing regulatory documents through the IRB and other research review boards and have the ability to handle a variety of clinical trial related regulatory responsibilities in accordance with University of Pennsylvania, GCP, ICF, and FDA guidelines.
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The Clinical Research Coordinator will coordinate all research visit activities for assigned projects (including processing and shipping blood and urine samples) and maintain research records in compliance with IRB and HIPAA regulations.
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This includes, but is not limited to, activities to advance health equity and disparities-focused study designs, community-academic partnerships and stakeholder engagement, inclusion and representativeness in CHOP clinical trials, interpretation and dissemination of findings in non-academic settings, and equitable translation (e.g., health services and policy research) of novel discoveries to advance patient care.
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All research faculty at CCRC receive the full support of the Center’s state-of-the-art research resources, including but not limited to comprehensive IT support; biomedical research core facilities; opportunities for clinical collaboration with MD Anderson Cancer Center at Cooper; and a fully staffed Research Office to assist with administration.
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We are seeking for our Philadelphia-based R&D laboratory a creative, motivated Research Associate/Scientist with expertise in cell biology laboratory techniques to contribute to the development of our novel, cell-penetrating peptide-based platform for biologics delivery.
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Description The Leukemia Research Team seeks a full-time, registered Clinical Research Nurse (CRN) to conduct studies involving a wide variety of investigational products and various sponsors.
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The Clinical Research Coordinator III works under limited supervision and runs portions of clinical trials, assists with orientation and training, obtains signature for informed consent, central lab management, data management, completes expectancy reports, monitors visit preparation, submits low institutional risk trials and tracks TJU IRB submission and approvals.
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The Division s clinical trial portfolio is further enhanced by an outstanding Phase I program, in academic partnership with the Sarah Cannon Research Institute (SCRI), and a strong and innovative Health Delivery Research effort.
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Founded by Emily Kramer-Golinkoff with family and friends in 2011, EE has awarded millions of dollars in research grants, launched a now-acquired CF gene therapy company, developed a patient registry and clinical trial matchmaking program to accelerate clinical trial recruitment, and led worldwide efforts to drive high-impact research and drug development.
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The fellow will contribute to a research project aiming at elucidating cellular and molecular mechanisms underlying genetic skeletal dysplasias, including achondroplasia and campomelic dysplasia, and at developing gene therapy approaches to alleviate the clinical manifestations of these disorders and improve the quality of life of affected individuals.
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As the chief clinical training site for the Lewis Katz School of Medicine at Temple University, the hospital provides a dynamic environment for high-quality care, teaching, and cutting edge research.
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The primary responsibilities for the Qualitative Research Intern will be to assist the MCFH Qualitative Research Coordinator with various components of research and evaluation activities involving the division's programs, namely the Vaccine Confidence Project.
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The In-Vivo Program Manager will play an integral part in overseeing vendor relationships related to clinical research into immunological pharmaceutical products. Keywords: Clinical Research Program Manager, Location: Philadelphia, PA - 19122.
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clinical research jobs Title: global medical director Company: Pfizer in Philadelphia, PA
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