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The Travel Clinical Research Coordinator primary responsibilities are to utilize Good Clinical Practices (GCP) in the process of screening, as well as enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
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Reviews study with principal investigator and/or clinical research coordinator to a budget outlining standard of care and research costs. In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies for feasibility and evaluates potential competition with other protocols prior to submitting study.
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The#Protocol Review and Regulatory Affairs department is looking for a Regulatory Startup Project Coordinator Summary: The Regulatory Startup Project Coordinator is responsible for shepherding clinical research projects through the study start up process to ensure activation time-lines meet (or exceed) institutional standards.
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The Clinical Research Coordinator will coordinate studies examining psychopathology during reproductive timepoints, including leading a study examining premenopausal neuroimaging markers of perimenopausal cognitive dysfunction.
$37,220 - $48,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Assistant Clinical Research Coordinator is responsible for coordinating and managing clinical trials including providing all aspects of protocol management, including creating study specific source documents, screening for patient eligibility, data collection and analysis, ensuring protocol compliance, adverse drug reaction reports, monitoring patient treatment and toxicities, laboratory and specimen submission, and maintenance of accurate and complete clinical research files.
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The Research Associate Clinical I-Data Manager will help the study team in preparing for monitoring visits and audits and ensure compliance with all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board ( IRB.
$17.24 - $27.59 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Clinical Research Coordinator I is responsible for ensuring quality adherence to protocol-specific and general regulatory requirements for translational research and clinical study efforts.
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Under the supervision of a Clinical Research Coordinator (CRC) or Principal Investigator (PI), the Assistant Clinical Research Coordinator will perform entry-level duties related to the support and coordination of several research studies, primarily the study “ Reimagining Precision Medicine Approaches to Alzheimer’s Disease Diagnosis.
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The AppearanCe Concerns, Eating, Prevention, and Treatment (ACCEPT) Lab at Auburn University is seeking a fulltime Research Assistant to work on a grant-funded study that is a clinical trial of virtual treatment for LGBTQ individuals with eating disorders.
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Join other professionals revolutionizing efficient and seamless study start-up to advance clinical trials. This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace.
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Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Study Start-up team. We have openings for clinical research coordinators to best match your experience level.
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Ensures site research quality by practicing in compliance with US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations through OSHA, CDC and HIPPA. Supports and adheres to US Oncology Compliance Program, to include the Code of Ethics Business Standards.
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Communicate to research participants, both orally and written, the difference between clinical activities and research activities in all study documents and research participant communications.
$60,608 - $66,458 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The evaluation includes a clinical interview and medical exam by a study physician specializing in memory problems, an assessment of memory and other thinking abilities, and a research blood draw.
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GENERAL SUMMARY/ OVERVIEW STATEMENT: The Massachusetts General Hospital Department of Psychiatry is seeking a full-time clinical research coordinator to assist with the operation of several ongoing research studies as well as future studies.
$33,000 - $47,000 a yearFull-timeExpandApply NowActive JobUpdated Today
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