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With guidance from a data request and review committee, ensure that HIPAA guidelines are strictly followed, and that all data provided is approved by the IRB. Act as a liaison between the investigator and the clinical data warehouse.
Part-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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ETL Developer - Build and implement ETL for new data workflows to integrate with the research data warehouse, both on-premises and establish/integrate with a Cloud presence at Microsoft Azure. Job Description SummaryThis director level position is responsible for managing the data services team responsible for developing and managing the extraction, transformation and loading of data to and from electronic medical records, data repositories, complex healthcare IT systems, and a data warehouse for research.
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Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator I is responsible for independently performing delegated tasks and procedures involving human subject research.
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Knowledge of healthcare data management concepts and regulatory/compliance policies (HIPAA, IRB, etc. Strong customer-facing experience, preferably with physicians, investigators, faculty/academic and research support staff.
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Current fields of Regenerative Aesthetics, Regenerative Sexual Medicine, and Regenerative Medicine are well established, clinical research facility requirements in place, and a tissue bank license are in place.
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Excellent knowledge of GxP, ICH guidelines, PhRMA code, FDA CFR, ISO clinical research ethics, HIPAA and patient privacy laws, EU Directive and other applicable local regulations. Knowledge of concepts of clinical research and drug development.
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DEPARTMENT ADDENDUM: Research Associate 1 works directly with Physicians, Clinical Research Coordinator, Research Program Administrator, or Research Nurse, or Principal Investigator to coordinate and/or implement the study and may serve as the point of contact for the external sponsors.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Laboratory Technician is responsible for assisting with document management, protocol related clinical assessments of research subjects, laboratory functions, and assisting in tasks of the Clinical Research Coordinators as it relates to the conduct of clinical trials.
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Ensuring research quality by practicing compliance and following the principles of Good Clinical Practice (GCP)/International Harmonization Conference (ICH), Health Insurance Portability and Accountability Act (HIPAA), Federal Drug Administration (FDA) policies and guidelines, and other applicable regulations (state and local.
$37.86 - $50.48 an hourFull-timeExpandUpdated 6 days ago - UpvoteDownvoteShare Job
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Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation). Minimum of 1 year of clinical laboratory experience in highly complex testing for those with BS/BA in Chemistry or Biology.
ExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Drafting and negotiating a broad range of agreements commonly needed in the medical device industry, including without limitation supply agreements, clinical trial agreements, research agreements, sales agreements, distribution agreements, consultant agreements.
$90,852 - $136,278 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Must have evidence of completion of training in Human Subjects Protection (HSP), Good Clinical Practices (GCP), HIPAA and other required research modules required by the IRB and by Parkland.
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Our research involves a broad set of projects ranging from microbiome and translational research to clinical trials. Additional responsibilities include working in close contact with gastroenterologists, research staff, clinical staff, Partners' Institutional Review Board (IRB), and fiscal/legal groups within and outside of Partners, as necessary.
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This portion of the position also includes managing clinic compliance documentation management for clinical educators and the graduate student clinicians they supervise (e.g., CPR, immunizations, HIPAA, Blood Borne Pathogen, etc.
$16.66 an hourFull-timeExpandUpdated 6 days ago
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