Clinical coordinator • chicago il
The Clinical Research Coordinator II is responsible for the overall management and implementation of an assigned set of multiple research protocols assuring efficiency and regulatory compliance.The...[internal_linking.show_more]
Coordinates all clinical research activities with moderate supervision.Adheres to the service values and principles of research ethics.The balance between patient-facing and administrative data tas...[internal_linking.show_more]
The clinical research coordinator position will be supporting clinical trials and research in the Division of Endocrinology.The CRC will work collaboratively with Lurie Children’s Hospital teammate...[internal_linking.show_more]
Coordinates all clinical research activities with minimal supervision.Adheres to the service values and principles as well as the principles of research ethics.Based on specific research program ne...[internal_linking.show_more]
BSD MED - Cardiology - Clinical Research Staff.The Section of Cardiology was founded in 1950 and has a proud history.We are now charting a new course that will propel us to the forefront of cardiov...[internal_linking.show_more]
Loretto Hospital is a safety-net hospital that serves more than 33,000 patients each year from Chicago’s Austin and surrounding communities.Established in 1923 as a not-for-profit community-focused...[internal_linking.show_more]
At Insight Hospital and Medical Center Chicago, we believe there is a better way to provide quality healthcare while achieving health equity.Our Chicago location looks forward to working closely wi...[internal_linking.show_more]
Coordinates and completes and day to day administrative and technical activities involved in concurrent and biomedical.The Research Coordinator also coordinates collection, analysis, processing, an...[internal_linking.show_more]
The Clinical Research Coordinator II coordinates all clinical research activities with moderate supervision.Adheres to the service values and principles of research ethics.The balance between patie...[internal_linking.show_more]
Manages daily operations of a biomedical &/or social-behavioral research study involving multidisciplinary teams of colleagues, sponsors & other external project stakeholders.Monitors study perform...[internal_linking.show_more]
At Insight Hospital and Medical Center- Chicago, we believe there is a better way to provide quality healthcare while achieving health equity.Our Chicago location looks forward to working closely w...[internal_linking.show_more]
BSD MED - Gastroenterology - Clinical Research Staff.The Section of Gastroenterology, Hepatology at The University of Chicago is consistently ranked among the best specialty nationally by U.With ne...[internal_linking.show_more]
Develops in-depth understanding of each study protocol to ensure all aspects of the protocol are adhered to in accordance with FDA, GCP, and ICH Guidelines.Serve as primary contact with research pa...[internal_linking.show_more]
Assists investigators and study team in the implementation, coordination, and conduct of clinical research activities.Adheres to the service values and principles as well as the principles of resea...[internal_linking.show_more]
The Clinical Quality Coordinator (CQC) RN works in collaboration with a broad group of stakeholders (nursing and medical directors, frontline clinical staff from all disciplines, Center for Quality...[internal_linking.show_more]
BSD MED - Genetic Medicine - Gilad Research Staff.The Section of Genetic Medicine continues to shape the future of personalized medicine with successful research programs focused on the quantitativ...[internal_linking.show_more]
WE ARE INSIGHT: Envisioning and implementing a holistic approach to neurological treatment is our goal, and our unique research and powerful solutions illuminate the path toward greater innovations...[internal_linking.show_more]
Envisioning and implementing a holistic approach to neurological treatment is our goal, and our unique research and powerful solutions illuminate the path toward greater innovations for the future ...[internal_linking.show_more]
Associate Clinical Study Coordinator.City of Hope's mission is to make hope a reality for all touched by cancer and diabetes.Founded in 1913, City of Hope has grown into one of the largest and most...[internal_linking.show_more]
Duties and Responsibilities
The Clinical Research Coordinator II is responsible for the overall management and implementation of an assigned set of multiple research protocols assuring efficiency and regulatory compliance. These studies will be conducted at the Loyola University Medical Center and satellites. He/she will work as part of a clinical trials research team and report to various Principal Investigators conducting clinical research in coordination with Clinical Research Nurse. Responsibilities include assisting in the preparation of initial study documents for IRB submission in compliance with all local, state and federal regulations; advise the IRB of amendment changes to the protocol and complete annual protocol renewals. Recruit, screen, assist in the informed consent process and enroll subjects in accordance with good clinical practice guidelines. Collect, record and maintain complete data files using good clinical practice in accordance to HIPAA regulations. He/she participates in data retrieval, reporting, and preparation of files and Case Report Forms for the various studies. The successful candidate will interact with subjects by scheduling diagnostic and research evaluation visits, perform study related assessments including collection of blood samples, processing and shipment. Maintain drug accountability, adequate study supplies and equipment. The coordinator will oversee subject compliance to the study protocol, obtain information from the study subject regarding any changes in their medications or adverse events and promptly report the findings to physicians for documentation in the subject’s medical record. Report all serious adverse events promptly to investigators, sponsors and the IRB. Protect the rights, safety and well-being of human subjects involved in the clinical trials.
