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Work where every*moment*matters. Every day, more than 40,000 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 Connecticut’s most comprehensive healthcare network. The Hartford HealthCare Cancer Institute focuses on offering our cancer patients an unparalleled network of coordinated services– 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 Institute’s focus to provide the newest and most effective approaches to cancer care within the community based on scientific evidence. The Oncology Clinical Research Coordinator (CRC) level I of Cancer Clinical Research Office (CCRO) is an integral member of the research team. This position is based in our Fairfield Region, St. Vincent’s 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 trial. The Clinical Research Coordinator (CRC) level I supports the protocol investigator(s) by providing research expertise; coordinates and facilitates protocol directed activities; at the investigator’s direction coordinates patient care within protocol parameters; communicates with care team (i.e. 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 process. · Under supervisor/manager direction and in conjunction with the Principal Investigator (PI) ensures protocol adherence and data integrity · Responsible for moderate to low complexity protocols, disease types and/or mild to moderate patient acuity (e.g., phase II/III studies, non-therapeutic studies), case load or routine enrollment · 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. · Conducts shared research visits in conjunction with the treating investigator and coordinates care with clinical team (i.e. nursing, supportive care, pharmacy, laboratory, radiology, etc.) to ensure protocol compliance and participant safety. · Responsible for identifying and reporting events (i.e. adverse events, serious events, non-compliance, deviations/violations) to the institutional review board (IRB) and other responsible bodies (i.e. hospital quality committee) · Proactively pre-screens to identify potential patients for protocol eligibility · Promotes research integrity and quality by participating in audit preparations and performing quality checks. · Supports site operations by traveling to investigator’s 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 and/or junior staff. *Education* · Bachelor’s Degree in science or related field, required. · Master’s Degree in science or related field, preferred. *Licensures or Certificates* · IATA or equivalent training, required/must be obtained within first month of hire. · Good clinical practice certification, required. · Clinical research professional certificate (i.e. ACRP, SOCRA, RAPS, etc.), preferred *Experience* The 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. S/he has exceptional attention to detail, excellent technical problem solving skills, ability to organize and prioritize multiple tasks and strong communication skills. S/he should have: · Two (2) years of direct clinical research experience · One (1) year oncology research experience, preferred · Two (2) year of patient facing responsibilities, preferred · Demonstrated commitment to quality service & care, team work, and HHC mission and values. · Demonstrated ability to exercise sound judgement We take great care of careers. With 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 – 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 work/life balance. Every moment matters. And this is*your moment.* **Job:** **Research* **Organization:** **Hartford HealthCare Corp.* **Title:** *Clinical Research Coordinator I - Oncology* **Location:** *Connecticut-Bridgeport-St Vincents Medical Center (10427)* **Requisition ID:** *25157945*