Clinical Research Coordinator - Danbury Hospital Clinical Trials department - Danbury, CT

Northwell is the largest not-for-profit health system in the Northeast, serving residents of New York and Connecticut with 28 hospitals, more than 1,000 outpatient facilities, 22,000 nurses and over 20,000 physicians. Northwell cares for more than three million people annually in the New York metro area, including Long Island, the Hudson Valley, Connecticut and beyond, thanks to philanthropic support from our communities. Northwell is New York State’s largest private employer with over 104,000 employees — including members of Northwell Health Physician Partners — who are working to change health care for the better. Title Clinical Research Coordinator - Danbury Hospital Clinical Trials - Full time/40 hours per week, 8-hour shifts, 8:00am - 4:30pm, Monday - Friday. Summary Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. Responsibilities include patient screening and recruitment, coordination of care of the research patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board (IRB). Coordinates studies in varied therapeutic areas including but not limited to Cardiovascular, Pulmonary, Gastroenterology, Neurology, Endocrinology, Dermatology and Rheumatology. Functions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporations. Responsibilities Screens patients for study participation e.g. reviews medical record, collaborates with medical & research staff, etc. and procures informed consent. Maintains accurate and thorough documentation on all source documents and case report forms (CRFs) for each study patient. Resolves all patient queries. Maintains communication with investigators/researchers, patients, internal and external collaborators (e.g. consulting physicians), sponsors, federal regulatory agencies, and other involved parties as required. Participates in investigator, coordinator, or study initiation meetings accordingly. Coordinates and participates in monitoring visits/audits with regulatory agencies or sponsors. Maintains current regulatory (GCP, HSR) and study specific required trainings. Prepares and submits all study protocols, consent forms, and other required documents to the Institutional Review Board (IRB). Educates hospital staff about protocols through in-services, written materials and one-on-one interaction, for each study and each patient, and for general marketing. Demonstrates flexibility in daily routine and effectively accommodates for the needs of the job (e.g. early or late patient enrollment). Performs procedures including EKG, Phlebotomy, blood and body fluid sampling, packing and shipment of human samples, body measurements and examinations within scope of practice and training, consistent with clinic and study specific policies/procedures and scope of care under the guidance of the supervisor. Fulfills all compliance responsibilities related to the position. Maintains and models Nuvance Health Values. Demonstrates regular, reliable and predictable attendance. Performs other duties as required. Education and Experience Requirements Bachelor's degree or Allied Health professional degree and three years job-related experience. Minimum 1-year clinical experience in medical field. Prefer: Clinical Research experience. Minimum Knowledge, Skills and Abilities Requirements Fluency in medical terminology. Knowledge of clinical trials, research and general medicine. Strong computer skills. Strong attention to detail and organizational skills. Outstanding interpersonal skills. License, Registration, or Certification Requirements Basic Life Support current or willing to take course. Valid Driver license. Prefer: Professional research certification. Salary Range $29.65 - $55.55 hourly (Pay per years of relative experience) #J-18808-Ljbffr