Clinical Research Coordinator

Job Description The Research Coordinator I will assist in the management of subjects on clinical trials and coordinate activities associated with clinical trials under the mentorship of a Research Coordinator II. Essential Functions Screens potential subjects for eligibility to prospective/observational trials through a careful review of the patient’s past medical history and a review of current findings against inclusion and exclusion criteria specific to a trial Assists with recruitment of subjects to prospective/observational trials through a variety of methods Maintains informed consents records of each patient for the duration of a study Procures, processes, and ships biospecimens per sponsor protocol and regulations Protects the rights, safety, and welfare of patients Strives to maintain harmonious relationships with clinic personnel, administrative staff, patients, their caregivers, and the public Reviews newly activated protocols, amendments, notices, suspensions, and terminations Responsible for maintaining current knowledge of the Code of Federal Regulations and International Council for Harmonization Guidelines Maintains required certification in Good Clinical Practice, Human Subjects Protections, and biological shipping training Serves as a liaison to multiple Tennessee Oncology departments, providers, and other personnel regarding research protocols and regulatory compliance Maintains a professional approach respecting the dignity and confidentiality of patients Maintains a good attendance record and reports to work on time Maintains a professional attitude and appearance Maintains Tennessee licensure as applicable Performs other duties as assigned Knowledge, Skills & Abilities Excellent verbal and written communication skills Excellent organization and follow‑up skills Ability to handle multiple priorities in a fast‑paced environment Ability to understand complex clinical trials protocols Ability to function in multi‑functional teams Microsoft Office product knowledge (Word, Excel, PowerPoint, etc.) Bilingual (English/Spanish) a plus Education & Experience Bachelor’s Degree or equivalent combination of education and experience required One year of relevant experience or work in a medical and/or laboratory facility required #J-18808-Ljbffr Astera Cancer Care