Clinical Research Coordinator II

at Loyola University Of Chicago in Maywood, Illinois, United States Job Description Position Details Position Details Job Title

CLINICAL RESEARCH COORDINATOR II

Position Number 8150821 Work Modality Is this request for the creation of a new Position (or the modification of an existing Position) to temporarily support the WorkDay ERP? Job Category University Staff Job Type Full-Time FLSA Status Non-Exempt Campus Maywood-Health Sciences Campus Department Name

ORTHOPAEDIC SURGERY

Location Code

CLINICAL RESEARCH OFFICE

(06124A) Is this split and/or fully grant funded? Yes Duties and Responsibilities Position Summary The Research Assistant supports the Department of Orthopaedic Surgery in the design, implementation, and administration of clinical research projects. This position works collaboratively with Principal Investigators (PIs), biostatisticians, residents, medical students, and other research staff to ensure regulatory compliance, data integrity, and the timely and efficient execution of departmental research and grant activities. Essential Duties and Responsibilities Regulatory and Compliance Prepare and submit new IRB applications in accordance with institutional policies and procedures. Submit and track amendments, continuing reviews, and study closures for active protocols. Draft, review, and maintain informed consent documents to ensure accuracy and regulatory compliance. Track and ensure completion of CITI and other required research trainings. Recognize and uphold ethical and compliance standards within assigned research activities. Research Administration Maintain departmental research administrative files, regulatory binders, and project documentation. Manage and update a comprehensive list of faculty and resident research publications. Prepare and submit research database requests and data use agreements (DUAs) for multi-institutional studies. Organize, review, and assist with grant submissions and grant budget preparation. Participate in project feasibility reviews and study initiation visits. Provide strategic guidance on study setup and implementation to ensure successful study launches. Assist with research-related reimbursements, supply procurement, and other administrative processes. Coordinate monthly research meetings for clinical subdivisions within the department. Data Management and Analysis Design and format research databases and surveys using REDCap and Excel platforms. Perform data entry, organization, quality assurance, and data cleaning to ensure completeness and accuracy. Collaborate with biostatisticians on study design, data analysis, and interpretation of findings. Study Coordination Conduct literature reviews and synthesize findings to support ongoing and new research projects. Screen potential participants, recruit subjects, and obtain informed consent under PI direction. Maintain secure shared files for on-site and remote project management. Coordinate study-specific meetings and maintain effective communication across study teams. Manuscript and Presentation Support Assist in the preparation of research findings, figures, and tables for reports, abstracts, and presentations. Format, edit, and submit scientific manuscripts to peer-reviewed journals and conference proceedings. Education and Training Train new research assistants and medical students in research processes and best practices. Organize logistics for the annual research course for incoming interns and summer medical students. Other Responsibilities Incorporate new processes, techniques, and technologies into research operations with Clinical Research Director or Chair approval. Perform additional duties as assigned by Principal Investigators. Maintain a positive, organized, and safe work environment. Performs other duties as assigned. Minimum Education and/or Work Experience Bachelors Degree OR equivalent training acquired via work experience or education 2-5 years of previous job-related experience

Qualifications Education and Experience Requirements Minimum:

Bachelor's degree in a scientific or health-related field.

Preferred:

Master of Public Health (MPH) or equivalent advanced degree.

Experience:

Minimum of 3-5 years of post-education research experience, preferably in an academic, clinical, or healthcare setting. Preferred Qualifications Hands-on experience conducting clinical research in an academic or healthcare environment. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook). Strong organizational, communication, and interpersonal skills, with the ability to collaborate effectively in multidisciplinary teams. Demonstrated ability to manage multiple projects and meet deadlines with accuracy and attention to detail. Experience with database design, data management, and research software (REDCap preferred). Familiarity with grant development, including proposal preparation and budget drafting. Experience with manuscript... For full info follow application link. To view full details and how to apply, please login or create a Job Seeker account