Erlanger Health System·Chattanooga, Tennessee
Provides administrative and clinical support for children's oncology research, including patient scheduling and specimen collection. Manages research files, databases, and ensures compliance with IRB and regulatory requirements.
Detail oriented, with ability to multi-task. Multi-skilled person dedicated to assisting in all aspects of research including administrative and clinical procedures. The Research Coordinator I assists primary research coordinators, nurses, managers and providers to care for patients. Performs routine clerical duties.
Education: Required: High School Diploma or GED equivalent
Graduate from an approved Medical Assistant program.
Required: 6 months - 1 year of experience in health care.
Phlebotomy training / experience preferred. Medical Terminology.
Preferred: additional certifications as required per clinical areas
Perform administrative and clerical duties, manage files and records, design forms, and other office procedures as required. Assist in Institutional Review Board (IRB) requirements for all studies. Maintains up-to-date records on research protocol patients. Assist with Scheduling and prepare patients for research visit. Collect routine laboratory specimens per study protocol or as directed by provider based on licensure and scope of practice as well as packaging and shipping of labs drawn. Coordinate with other departments (i.e.: radiology, pathology, surgery, clinical laboratory) for the pick-up of research specimens/scans housed in that area for processing and shipment per study guidelines, under supervision Observe and report patients� signs or symptoms based on licensure and scope of practice. Assist with patient examinations based on licensure and scope of practice. Operate office medical equipment based on licensure and scope of practice. Assist in maintaining studies, databases (EDC, registries, etc.) and data entry. Resolve queries under supervision. Maintains all filing for Research Department. Copies/faxes/mails documents as required. Assist in preparing for research audits/site visits by gathering necessary charts, images, regulatory binders, and securing a room for the visit as needed. Excellent oral and written communications skills, ability to relate well to people of a broad socioeconomic mix, with sensitivity to the patient. Ability to work in a typical office setting with some stressful situations, personal flexibility; moderate sitting, stooping, bending, and moderate work at word processing screen required.
Market context
In Tennessee, Research Coordinator I roles in children's oncology are typically in steady demand at hospitals, academic medical centers, and research programs that support pediatric trials. These positions are competitive because employers often want candidates who can manage protocol details, work with families and clinical teams, and quickly complete required certifications such as CITI, IATA, and CCRP. Review the original posting carefully and, if you are close to the experience threshold, highlight any healthcare exposure and your readiness to obtain the listed credentials; the requirements and benefits here are AI-summarized from the source job description, which can save you time during your search.
Nurse Tech 1 WW3 Renal PRN Nights **Nursing Student in the last year of Nursing School**
RN eSTAR Surgical Admit Unit- Fulltime Nights
Nurse Tech 1- NW9s Trauma Surgical PRN **Nursing student in the last year of Nursing School