CLINICAL RESEARCH COORDINATOR
School of Medicine
Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,200 staff, the Duke University School of Medicine along with the Duke University School of Nursing, and Duke University Health System comprise Duke Health, a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Health Integrated Practice, Duke Primary Care, Duke Home Care and Hospice, Duke Health and Wellness, and multiple affiliations. Be You. The Department of Surgery is looking for a Clinical Research Coordinator to join our team. This critical role will participate in the day-to-day operations of clinical research for the Cardiovascular and Thoracic Division. The Surgery Office of Clinical Research (SOCR) is staffed with experienced individuals who are dedicated to patient safety while conducting innovative research with the hope of advancing medicine and improving clinical care. Minimum Requirements:- Completion of an Associate's Degree
- A minimum of two years of relevant research experience. A Bachelor's degree may substitute for two years required experience.
Preferred Qualifications:
- Can easily use computing software and web based applications (e.g., Microsoft Office products and internet browsers).
Other Requirements:
- Responsible for all aspects of managing and documenting Investigational Product (IP); including arrival, storage, tracking, and provision to research participants. Serves as the primary liaison with sponsors, Investigational Drug Service (IDS), and other parties as necessary. Follows protocol schema for randomization and blinding and unbinding.
- Prepares for and provides support for study monitoring and audit visits, including support for the reviewer. Addresses and corrects findings.
- Conducts activities for study visits in compliance with the protocol.
- Conducts and documents consent for participants for all types of studies, including those that are complex in nature and require any orders in Maestro Care.
- Ensures accuracy and completeness of data for all studies, including those that are complex in nature. Recognizes data quality trends and escalates as appropriate. May develop tools for, and train others in, data quality assurance procedures.
- Collects appropriate information to determine whether the study teams participation in a specific trial is feasible. May make feasibility recommendations.
Choose Duke.
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