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Candidate will be responsible for patient chart review; lab processing, EKG and other duties such as ambulatory blood pressure monitor and pulse wave velocity; perform basic laboratory assay techniques; manage inquiries related to the research studies including billing; maintain daily log books of research activity; follow strict study protocol and correspond regularly with the IRB.
$36,401 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Perform group-specific regulatory activities, such as site selection visits, document completion (site selection questionnaires, 1572's and financial disclosure forms), and IRB and IND report completion (with investigator input), including AE reports, deviations, CRs and modifications.
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The Clinical Research Coordinator A will recruit and screen patients as outlined in research protocols, will coordinate all research visit activities for assigned projects (including processing and shipping blood and urine samples), and will assist in the maintenance of research records in compliance with IRB and HIPAA regulations.
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Perform other duties as may be assignedQUALIFICATIONS: Effective problem solving abilities; effective communication and writing skills; strong organizational and time management skills; flexible and able to multi-task; demonstrated ability to work as part of a team, as well as independently; knowledge of IRB and human research protection regulations.
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Responsible for completing and maintaining all study documents, in compliance with IRB , Cooper University Hospital, Sponsor and FDA requirements. Coordinates planning study conduct, submission of all IRB regulatory documents/amendments, preparation and conduct of studies by residents and faculty.
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Responsible for overall management of the trial(s) to ensure compliance with study protocol, FDA, NIH and IRB policies. Responsible for overall management of the trial(s) to ensure compliance with study protocol, FDA, NIH and IRB policies.
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Primary responsibilities include the coordination of study enrollment; oversight of study protocols; and submission of research activities per IRB regulations. Additional responsibilities include working independently to drive day-to-day research activities; monitoring and tracking expenditures; supporting multiple active protocols simultaneously; and working with multiple investigators while adhering with FDA, IRB, Pennsylvania, and related regulations.
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BSN or ECFMG certification. New Jersey RN license or ECFMG Certification. Minimum two years ObGyn clinical research experience preferred; epidemiology background helpful. Responsibility of ensuring that research in the Department of OB/GYN is promoted, facilitated and conducted in an ethical and responsible manner.
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Effective problem solving abilities; effective communication and writing skills; strong organizational and time management skills; flexible and able to multi-task; demonstrated ability to work as part of a team, as well as independently; knowledge of IRB and human research protection regulations.
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Basic knowledge of Institutional Review Board (IRB) processes and policies. The Clinical Research Associate (CRA) in the Protocol Support Office [PSO] performs comprehensive monitoring of clinical research studies within the Division of Oncology and the Center for Childhood Cancer Research (CCCR) under the guidance of the program manager.
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Short Description Responsibility of ensuring that research in the Department of OB/GYN is promoted, facilitated and conducted in an ethical and responsible manner. Discover why Cooper University Health Care is the employer of choice in South Jersey.
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Knowledge of human subjects research, patient privacy, and data use considerations required; working knowledge of IRB submission and review process is a plus. Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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Assist with Institutional Review Board (IRB) filings. Complete regulatory filings with IRB, OCR. The Clinical Research Coordinator A for the Chirinos Lab will be responsible for conducting study visits and data management for HFpEF related studies.
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Runs portions of clinical trials from startup to closeout, including protocol coordination (screening, recruiting, enrolling, consenting), feasibility planning, data management, biological specimen management, preparation for monitoring visits, and regulatory and/or IRB document preparation.
Full-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Promptly documents and reports any observed protocol/trial issues to the IRB, OR, and PI. Prepares and submits IRB documents under the direction of the PI and prepares regulatory documents to be sent to the Sponsor; assists in addressing documents and contracts through IRB process and approval; under direction of PI may draft various communications with Sponsor.
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irb job in Philadelphia, PA
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