Clinical Research Coordinator (Radiology)
Saint Louis UniversityAbout the role
Who is Saint Louis University? Founded in 1818, Saint Louis University is one of the nation’s oldest and most prestigious Catholic universities. SLU, which also has a campus in Madrid, Spain, is recognized for world-class academics, life-changing research, compassionate health care, and a strong commitment to faith and service.
JOB SUMMARY
The Clinical Research Coordinator (Radiology) will be responsible for oversight of clinical trials for the SLU School of Medicine which include screening, recruiting and enrolling subjects, conducting subject research visits, providing technical and administrative expertise in the preparation and administration of investigational products (imaging & therapy) in research subjects, data collection and data entry, detailed source documentation, maintenance of study documents, and review of budgets in coordination with the Clinical Trials Office. This position will liaise with core offices including the Clinical Trials Office, SLU Institutional Review Board, SLU Radiation Safety Committee & SSM Research Compliance Office as well as industry sponsors and associated Contract Research Organizations (CROs)/vendors. The position will require the ability to collaborate with departmental as well as non-departmental team members and other research professionals in a manner consistent with St. Louis University's core values.
PRIMARY JOB RESPONSIBILITIES
Screens, recruits, and enrolls patients into research studies in accordance with good clinical practice
Schedules and conducts research study visits
Provides technical and administrative expertise in the preparation and administration of investigational products
Records and documents study visits utilizing ALCOA+ principles
Performs data entry and query resolution
Collects, processes, and ships biospecimens
Maintains accurate and complete study documents
Liaises with Clinical Trials Office, SLU Institutional Review Board, SLU Radiation Safety Committee & SSM Research Compliance Office
Liaises with industry sponsors, CROs and vendors
Attends meetings (i.e. Site Selection, Site Initiation, Investigator Meetings, and departmental meetings)
Performs other duties as assigned
KNOWLEDGE, SKILLS, AND ABILITIES
Knowledge of regulations and guidelines related to clinical research
Knowledge of clinical research terminology and multiple medical conditions
Knowledge of GE Centricity, EPIC, Clinical Conductor CTMS and other University Electronic Data Systems
Proficient computer skills using Microsoft Office platform
Strong interpersonal and customer service skills
Excellent time management, organizational and multitasking skills
Ability to maintain confidentiality
MINIMUM QUALIFICATIONS
Bachelor’s degree
Two or more years of related work experience
Certified Nuclear Medicine Technologist (CNMT)
PREFERRED QUALIFICATIONS
Clinical research professional certification
Function
Clinical ResearchScheduled Weekly Hours:
40Saint Louis University is an equal opportunity/affirmative action employer. All qualified candidates will receive consideration for the position applied for without regard to race, color, religion, sex, age, national origin, disability, marital status, sexual orientation, military/veteran status, gender identity, or other non-merit factors. If accommodations are needed for completing the application and/or with the interviewing process, please contact Human Resources at 314-977-5847.
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