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Use programs such as clinical computer systems, including Composite Health Care System (CHCS-I) and Gensis, for consultation, reporting, exchange of information, orientation, support in the performance of assigned duties, and to guide patients through a research protocol.
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ResponsibilitiesA day in the life of a Lead Clinical Research Nurse at Hackensack Meridian Health may include:Works together with and oversees all assigned Clinical Research Nurses Interacts with regulatory specialists and principal investigators and sub-investigators on all regulatory issues and changes within the protocol.
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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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Preferred Qualifications At least one year of previous experience as a clinical research coordinator or equivalent combination of experience / training Fluent in spoken and written Spanish and/or Arabic About UCSF The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care.
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Licensures and Certifications: California Clinical Laboratory Scientist (CLS) License required. Two years of experience working as a clinical laboratory scientist (CLS) in a medical laboratory preferred.
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Clinical Research Coordinator, Norwalk, CT. Clinical Research Coordinator. Reports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies.
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A bachelors degree from an accredited university or college in biology, physiology, chemistry, or related field is required; however, animal research experience will be taken into consideration in lieu of a degree on a case-by-case basis.
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The Clinical Research Physician will serve as a Principal Investigator and/or Sub-Investigator for clinical trials, holding responsibilities and accountabilities for overseeing all clinical and medical aspects of study conduct.
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Education Certifications, licenses, or degrees as determined by the needs of the research projects, such as, registered nurse, nurse practitioner, certified mental health therapist/specialist, MSW, pharmacist, physical therapist, certified health education specialist, clinical psychologist, acupuncturist.
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Overview The Research Nurse in collaboration with the physician, is responsible for the implementation and evaluation of clinical research in their specific program/area. The CRN has expert knowledge of cancer as a disease process, cancer treatment modalities (or comparable knowledge for a non-oncology area, e.g. infection control) and the process of conducting medical clinical research.
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About the NCI Center for Cancer ResearchThe Center for Cancer Research (CCR) is home to nearly 250 basic and clinical research groups located on two campuses just outside of Washington, CCR is part of the National Cancer Institute (NCI) and makes up the largest component of the research effort at the National Institutes of Health (NIH.
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Responsibilities:- Ensure compliance with regulatory requirements for working with animals in biomedical research, including the Animal Welfare Act & Regulations, the Guide for the Care and Use of Laboratory Animals, local policies, and other applicable regulations.
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Must have a demonstrated, thorough knowledge of animal anatomy, medicine, physiology and pathology as well as working knowledge of histology, clinical pathology, surgery, pharmacology, bacteriology, virology, parasitology, mycology, biochemistry and other related disciplines.
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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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The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
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clinical research jobs Title: animal health Company: University Of Alabama At Birmingham
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