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Work with the start-up team, CTMS and UW Clinical Trials Office (CTO) to review billing calendars, Medicare Coverage Analysis (MCA), and financial entries and bill routing. Knowledge of the Medicare Clinical Trials Policy and other federal, state, and institutional clinical research regulations.
$4,409 - $5,929 a monthTemporaryExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Regulatory Coordinator Oncology Clinical Research Unit [CRU] Brain TUMOR CLINICAL Research Program [BTC] Position Description, Occupational Summary Perform regulatory and safety processes for multiple, complex oncology clinical trials and research studies including Investigational Products [IP] for the Duke Cancer Institute’s [DCI] TEAM Clinical Research Program [BTC.
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The Clinical Research Coordinator works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
$85,000 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Position The Rapid Cycle Analytics (RCA) Lead Data Scientist role sits within the Clinical Data Science and Evidence (CDSE) team, which is part of CMR. This role interfaces with internal stakeholders from Health Economics and Outcomes Research (HEOR), Real-World Evidence (RWE), Medical Affairs, Clinical Trials Operations, Market Access, and a few other teams to respond to quick turnaround data analytics requests.
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Join other professionals revolutionizing efficient and seamless study start-up to advance clinical trials. Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF.
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We are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida.
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Graduate or fellowship training in a relevant field, for example, clinical epidemiology, clinical pharmacology, clinical trials, is preferred. The Canadian Cancer Trials Group (CCTG) is a cooperative oncology group that designs and administers clinical trials in cancer therapy, supportive care, and prevention across Canada and internationally.
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The Clinical Research Associate (CRA) II is responsible for monitoring clinical study sites either onsite at investigative sites or remotely to ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements.
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The Case Manager works closely with the Lead Case Manager, Program Directors, and the Clinical, Medical, Education, Youth Care Worker departments. Complete and submit reunification packets for initial review to Lead Case Manager or Designee (if applicable.
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The Utilization Review Nurse will be working on Medicare Advantage cases and will be responsible for reviewing medical records to ensure medical necessity for members. A prestigious healthcare organization is seeking for a talented RN Utilization Review Nurse to join their organization on a remote basis.
$70 an hourTemporaryExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Completed at least 36 months(or 35 hours per week full time equivalent of 5,460 hours) clinical medical dosimetry experience under the direction of a certified medical dosimetrist or a medical physicist.
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Review records, consult with referring agency representatives (law enforcement, DCFS, state foster care licensing investigators, attorneys, judicial officials), interview primary caregiver for history relevant to the allegations (e.g., home environment, family relationships, alleged victim’s physical/mental health, etc.
$41 an hourPart-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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We seek outstanding candidates with teaching experience in the following: industry experience in entrepreneurship, drug discovery and development, cell and molecular biology, genetics, biochemistry, microbiology, laboratory instruction, biotechnology finance, regulatory affairs, clinical trials, project management, or manufacturing.
$3,527 a monthPart-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Review OCFS records to support effective and case-specific clinical consultation. Spurwink is partnered with Maine's Department of Health and Human Services to provide clinical consultation and support services to the Office of Child and Family Services - this position directly supports OCFS District 3, Lewiston.
$52,000 - $62,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Interaction: This role interacts with numerous teams, including health economic and outcome research, market access, commercial operations and strategy, payer and employer relations, business development and clinical trials, data and statistical programmers, biostatisticians, project management, IT and external vendors.
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review clinical trials jobs Title: manager clinical Company: Hca Healthcare
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