Clinical Research Coordinator I - Oncology
Clinical Laboratory Partners
Work where every moment mattersEvery day more than Hartford HealthCare colleagues come to work with one thing in common Pride in what we do knowing every moment matters here We invite you to become part of Connecticutrsquos most comprehensive healthcare networkThe Hartford HealthCare Cancer Institute focuses on offering our cancer patients an unparalleled network of coordinated servicesndash all under one roof Our system of care includes a truly integrated team with the most talented experienced and compassionate caregivers and physicians backed by the latest cutting edge technology This includes our new MSK Care Partners program that furthers the Cancer Institutersquos focus to provide the newest and most effective approaches to cancer care within the community based on scientific evidenceTheOncology Clinical Research Coordinator CRC level Iof Cancer Clinical Research Office CCRO is an integral member of the research team This position is based in our Fairfield Region St Vincentrsquos Medical Center and will support a portfolio of cancer research studies In compliance with all regulatory institutional and departmental requirements performs patient screening data collection and data entry for research protocols databases and projects within Hartford Healthcare Cancer Institute and ensures the data quality and integrity for each clinical trialThe Clinical Research Coordinator CRC level I supports the protocol investigators by providing research expertise coordinates and facilitates protocol directed activities at the investigatorrsquos direction coordinates patient care within protocol parameters communicates with care team ie infusion nursing pharmacy pathology etc to ensure proper conduct protocol compliance and human subject protections The CRC presents trial concepts and details and participates in the informed consent processmiddot Under supervisormanager direction and in conjunction with the Principal Investigator PI ensures protocol adherence and data integritymiddot Responsible for moderate to low complexity protocols disease types andor mild to moderate patient acuity eg phase IIIII studies non therapeutic studies case load or routine enrollmentmiddot Responsible for accurate and timely source documents data collection documentation entry and reporting including timely response to sponsor queries Responsible for compiling and reporting on each study including information related to protocol activity accrual data workload and other research information present this information at regular research staff meetings middot Conducts shared research visits in conjunction with the treating investigator and coordinates care with clinical team ie nursing supportive care pharmacy laboratory radiology etc to ensure protocol compliance and participant safetymiddot Responsible for identifying and reporting events ie adverse events serious events non compliance deviationsviolations to the institutional review board IRB and other responsible bodies ie hospital quality committeemiddot Proactively pre screens to identify potential patients for protocol eligibilitymiddot Promotes research integrity and quality by participating in audit preparations and performing quality checksmiddot Supports site operations by traveling to investigatorrsquos meetings trainings or to other Hartford HealthCare research sites participates in workgroups task forces serves as subject matter expert to comment on policies training materials or tools participates in subject specific training and mentorship of new andor junior staffWork where every moment mattersEvery day more than Hartford HealthCare colleagues come to work with one thing in common Pride in what we do knowing every moment matters here We invite you to become part of Connecticutrsquos most comprehensive healthcare networkThe Hartford HealthCare Cancer Institute focuses on offering our cancer patients an unparalleled network of coordinated servicesndash all under one roof Our system of care includes a truly integrated team with the most talented experienced and compassionate caregivers and physicians backed by the latest cutting edge technology This includes our new MSK Care Partners program that furthers the Cancer Institutersquos focus to provide the newest and most effective approaches to cancer care within the community based on scientific evidenceTheOncology Clinical Research Coordinator CRC level Iof Cancer Clinical Research Office CCRO is an integral member of the research team This position is based in our Fairfield Region St Vincentrsquos Medical Center and will support a portfolio of cancer research studies In compliance with all regulatory institutional and departmental requirements performs patient screening data collection and data entry for research protocols databases and projects within Hartford Healthcare Cancer Institute and ensures the data quality and integrity for each clinical trialThe Clinical Research Coordinator CRC level I supports the protocol investigators by providing research expertise coordinates and facilitates protocol directed activities at the investigatorrsquos direction coordinates patient care within protocol parameters communicates with care team ie infusion nursing pharmacy pathology etc to ensure proper conduct protocol compliance and human subject protections The CRC presents trial concepts and details and participates in the informed consent processmiddot Under supervisormanager direction and in conjunction with the Principal Investigator PI ensures protocol adherence and data integritymiddot Responsible for moderate to low complexity protocols disease types andor mild to moderate patient acuity eg phase IIIII studies non therapeutic studies case load or routine enrollmentmiddot Responsible for accurate and timely source documents data collection documentation entry and reporting including timely response to sponsor queries Responsible for compiling and reporting on each study including information related to protocol activity accrual data workload and other research information present this information at regular research staff meetings middot Conducts shared research visits in conjunction with the treating investigator and coordinates care with clinical team ie nursing supportive care pharmacy laboratory radiology etc to ensure protocol compliance and participant safetymiddot Responsible for identifying and reporting events ie adverse events serious events non compliance deviationsviolations to the institutional review board IRB and other responsible bodies ie hospital quality committeemiddot Proactively pre screens to identify potential patients for protocol eligibilitymiddot Promotes research integrity and quality by participating in audit preparations and performing quality checksmiddot Supports site operations by traveling to investigatorrsquos meetings trainings or to other Hartford HealthCare research sites participates in workgroups task forces serves as subject matter expert to comment on policies training materials or tools participates in subject specific training and mentorship of new andor junior staffEducationmiddot Bachelorrsquos Degree in science or related field requiredmiddot Masterrsquos Degree in science or related field preferredLicensures or Certificatesmiddot IATA or equivalent training requiredmust be obtained within first month of hiremiddot Good clinical practice certification required middot Clinical research professional certificate ie ACRP SOCRA RAPS etc preferredExperienceThe CRC is expected to consistently complete tasks with minimal supervision demonstrate the ability to understand and implement scientific protocols and have a strong working knowledge of applicable regulations and best practices with regard to site logistics She has exceptional attention to detail excellent technical problem solving skills ability to organize and prioritize multiple tasks and strong communication skills She should havemiddot Two years of direct clinical research experiencemiddot One year oncology research experience preferredmiddot Two year of patient facing responsibilities preferred middot Demonstrated commitment to quality service care team work and HHC mission and valuesmiddot Demonstrated ability to exercise sound judgementWe take great care of careersWith locations around the state Hartford HealthCare offers exciting opportunities for career development and growth Here you are part of an organization on the cutting edge ndash helping to bring new technologies breakthrough treatments and community education to countless men women and children We know that a thriving organization starts with thriving employees we provide a competitive benefits program designed to ensure worklife balance Every moment matters And this is your momentEducationmiddot Bachelorrsquos Degree in science or related field requiredmiddot Masterrsquos Degree in science or related field preferredLicensures or Certificatesmiddot IATA or equivalent training requiredmust be obtained within first month of hiremiddot Good clinical practice certification required middot Clinical research professional certificate ie ACRP SOCRA RAPS etc preferredExperienceThe CRC is expected to consistently complete tasks with minimal supervision demonstrate the ability to understand and implement scientific protocols and have a strong working knowledge of applicable regulations and best practices with regard to site logistics She has exceptional attention to detail excellent technical problem solving skills ability to organize and prioritize multiple tasks and strong communication skills She should havemiddot Two years of direct clinical research experiencemiddot One year oncology research experience preferredmiddot Two year of patient facing responsibilities preferred middot Demonstrated commitment to quality service care team work and HHC mission and valuesmiddot Demonstrated ability to exercise sound judgementWe take great care of careersWith locations around the state Hartford HealthCare offers exciting opportunities for career development and growth Here you are part of an organization on the cutting edge ndash helping to bring new technologies breakthrough treatments and community education to countless men women and children We know that a thriving organization starts with thriving employees we provide a competitive benefits program designed to ensure worklife balance Every moment matters And this is your moment
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