OneOncology
Location
Mount Juliet, Tennessee
This role involves assisting with various clinical research activities under mentorship, including screening potential subjects for eligibility against trial criteria and managing informed consent records. The coordinator will also be responsible for procuring, processing, and shipping biospecimens according to protocol and regulations.
Candidates must possess a Bachelor's Degree or an equivalent combination of education and experience, along with at least one year of relevant experience in a medical or laboratory facility. Essential abilities include excellent communication, strong organizational skills, the capacity to handle multiple priorities, and knowledge of complex clinical trial protocols.
This position works closely with the research team to learn and assist with a variety of clinical research activities. The Research Coordinator I will assist in the management of subjects on clinical trials and coordinating activities associated with clinical trials under the mentorship and guidance 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 Maintain 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 Thank you for your interest in Tennessee Oncology. People like yourself have helped us grow into one of the largest and most influential oncology practices in the country. Our front line heroes are beloved by our patients and their families. Caring for cancer patients is a privilege.
