University of Colorado Anschutz Medical Campus 

Department: Department of Physical Medicine and Rehabilitation

Job Title: Research Services Intermediate Professional

Position #:00846569 – Requisition #:39533

Job Summary:

We seek a highly motivated, enthusiastic, curious, organized, detail-oriented, and considerate person to become a full-time Intermediate Clinical Sciences Professional in the B4 Health Lab, in the Department of Physical Medicine and Rehabilitation. The Lab provides an exciting opportunity to participate in basic and translational work on research projects related to the connections between the Brain, Body, Biome, and Behavior to enhance physical and mental health through investigation and education.

Intermediate Clinical Sciences Professionals perform clinical research related functions which include participant-oriented research or research conducted with human subjects. Participant-oriented research includes mechanisms of human disease, therapeutic interventions, clinical trials, or development of new technologies. Intermediate Professionals may also assist with epidemiologic and behavioral studies and/or outcomes research and health services research. Work involves creating, integrating, applying and sharing knowledge. At the intermediate level, duties may be more limited in scope and are performed with guidance and direction from other professionals. Intermediate Professionals are responsible for exercising discretion, analytical skill, personal accountability and responsibility in a wide range of areas including academic, administrative, managerial and student services functions.

Core Responsibilities:

• Project/Trial Coordination & Operations — Serve as Primary Coordinator across multiple studies, overseeing day-to-day project operations while independently mastering protocols, informed consent forms, and all essential study documents to ensure procedures are performed in full compliance with regulatory standards.

• Participant Recruitment & Eligibility — Lead recruitment efforts including pre-screening, phone contacts, and in-person interviews; review inclusion/exclusion criteria; obtain medical histories and current medications; and confirm participant eligibility prior to enrollment.

• Informed Consent & Scheduling — Conduct and thoroughly document the informed consent process, and coordinate participant scheduling by arranging necessary space and clinical support resources including physicians, nursing, laboratory, radiology, and pharmacy.

• Data Collection & Regulatory Compliance — Accurately collect, code, and analyze study data while maintaining detailed records in accordance with FDA requirements, study protocols, and applicable SOPs; ensure all supplies and equipment are stocked and fully operational.

• Process Improvement & Quality Assurance — Support team leads and management in developing and implementing procedures, SOPs, and quality improvement initiatives to enhance operational efficiency and maintain the highest standards of research practice.

Additional Duties & Responsibilities:

• Attend lab and study team meetings.

• Data entry and quality assurance reviews in REDCap and Excel.

This description is a summary only and is describing the general level of work being performed, it is not intended to be all-inclusive. The duties of this position may change from