RADIOLOGY SERVICES RESEARCH COORDINATOR III

Radiology Services Research Coordinator III

The Radiology Services Research Coordinator III (RSRC III) is a highly skilled role responsible for supporting clinical research by coordinating imaging components of studies that require protocol specific imaging procedures. The position plays a critical role in maintaining data accuracy, ensures adherence to imaging requirements and regulatory standards, and supporting the successful execution of research protocols. It provides core support to the department, independently coordinating departmental tasks and special projects as assigned by the manager. Working collaboratively with clinical research coordinators, study investigators, data managers, radiologists, technologists, sponsors and imaging core labs, the role ensures adherence to imaging requirements and regulatory standards. The role independently develops departmental guides and imaging research training materials, continually looks for way to improve team tasks, process workflows and efficiencies, and serves as a mentor to less-experienced team members. This position is the top level of the Research Services Research Coordinator career path. This is a fully proficient role performing all RSRC core support functions. Workload is more complex and comprehensive than lower-level radiology services coordinators.

Requirements:

Education:

Associate's degree in Clinical Research, Health Sciences, or a related field is preferred. A High School Diploma or GED with an additional two (2) years of experience will be considered in lieu of a degree.

Experience:

Minimum of Three (3) years of experience in radiology, research, or a healthcare related field is required. Five (5) total years of experience with a HS diploma/GED.

Licenses/Certifications:

Clinical Research Certification from SOCRA or Clinical Research Certification CCRC from ACRP preferred

Training Required :

Must possess strong verbal and written communication skills, along with excellent interpersonal abilities to effectively collaborate with staff and other healthcare professionals. Must demonstrate the ability to prioritize tasks, self-manage workload, and maintain productivity while working under deadlines and managing high work volumes. Must possess ability to manage tasks independently. Must possess analytic skills with initiative to problem solve and improve processes.

Preferred Experience:

Proficiency with Microsoft Office (e.g. Excel, Word) and Adobe Acrobat,• Familiarlity with electronic medical record (EMR) systems such, as PowerCharts• Experience using clinical trial management systems (CTMS), such as OnCore• Knowledge of radiology systems (e.g. PACS) or other data entry platforms• Prior experience working with clinical trials is strongly preferred• Familiarity with confidentiality requirements and security of subject research data• Previous experience in radiology, a medically related field, or a demonstrated understanding of medical terminology is also preferred• Prior experience in an oncology setting is a plus

Salary Range

$22.74 - $34.68

Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.

We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.

If you have the vision, passion, and dedication to contribute to our mission,

then we have a place for you!