IROC Philadelphia (Imaging) QA Center, at the ACR Research center in Philadelphia, IROC Philadelphia (RT) QA Center, at the ACR Research center in Philadelphia, IROC Rhode Island QA Center in Lincoln, Rhode Island, administered by the University of Massachusetts Medical School IROC Ohio QA Center, at Ohio State University Wexner Medical Center and James Comprehensive Cancer Center. IROC Houston QA Center, at the MD Anderson Cancer Center thereby assuring high quality data for clinical trials designed to improve the clinical outcomes for cancer patients worldwide." Centers The Imaging and Radiation Oncology Core (IROC) is a center for the evaluation of data produced by clinical trials funded by the National Cancer Institute, as part of the National Clinical Trials Network "to provide integrated radiation oncology and diagnostic imaging quality control programs. Quality assurance, Clinical trials, cancer research Quality standards, event notability guideline, or encyclopedic content policy. Please expand this article with properly sourced content to meet Wikipedia's This position has no patient contact.This article reads like a press release or a news article and may be largely based on routine coverage. QARC provides radiation therapy and diagnostic imaging services to sponsors conducting cancer clinical trials. This position is located at the QARC data center in Lincoln, RI. Usual office environment, laboratory, medical, surgical, and off campus study sites Under the direction of the Principle Investigator or designee Good writing skills with the ability to compose correspondence.Excellent interpersonal and oral communication skills.High degree or organizational and analytical ability to manage data collection and protocol adherence.Excellent computer skills including: proficiency in word processing proficiency in relational databases.Ability to read and understand complex protocols.1-3 years experience in on-study data management and data collection in a research organization.Bachelor’s degree in a scientific or health care field, or equivalent experience.Participate in the documenting work procedures specific to new studies.Participate in regularly held Protocol Review Committee meetings.Present current status of studies assigned Participate in all office staff meetings. Adheres to Good Clinical Practice (GCP) guidelines and all human subject protection practices.Serves as a resource to physician and nurses to locate information for special reports and treatment decisions.Run quality control checks on data prior to transfer Provide data to study investigators as requested and submits data for analysis.Ensure that protocol document has current amendments.Keep principal investigator and research nurse aware of any issues on compliance Identify and resolve issues with protocol compliance. Review protocol requirements with physicians and research nurses.Assure that cases are being finalized and reviewed by appropriate clinician Monitor strict adherence to protocols.Maintain effective working relationships with research nurses and investigators participating in the study.Track and maintain accurate data of studies, accrual, and patient status activity in database.Monitor status of all studies in database and ensures that all patient data (on-study and follow-up) are submitted, and respond to data queries from sponsoring organization, in a timely manner.Monitors quality and timelines of data submissions Extract and transcribe treatment data from hospital and clinical records required to complete study patient’s record and sponsor’s case report forms.
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