Research Services Clinical Sciences Professional OPEN RANK (Entry – Senior) Onsite

University of Colorado•Aurora, CO

2d•$49,899 - $78,665•Onsite

About The Position

The B4 Health Lab is seeking dedicated researchers to join their full-time team. This role focuses on the interconnectedness of the Brain, Body, Biome, and Behavior to improve physical and mental health. It is an active, hands-on position involving multiple aspects of human subjects clinical research across various studies, suitable for individuals who excel in a fast-paced, detail-oriented environment. This is not a wet lab or bench science position.

Requirements

Bachelor's degree
U.S. Citizenship or Permanent Resident status (required due to funding restrictions)
At least one (1) year of human clinical research administration experience, including familiarity with research methods, protocols, data collection, and analysis (for Intermediate Level)
At least two (2) years of human clinical research administration experience, including familiarity with research methods, protocols, data collection, and analysis (for Senior Level)

Nice To Haves

One (1) year of research administration experience, including fundamental knowledge of research methods, protocols, data collection, and analysis (for Entry Level)
Master’s degree in science or health related field (for Intermediate and Senior Levels)
Two (2) years of research administration experience, including skilled knowledge of research methods, protocols, data collection, and analysis (for Intermediate Level)
Four (4) years of research administration experience, including advanced knowledge of research methods, protocols, data collection, and analysis (for Senior Level)
Experience in REDCap surveys and data entry
Strong working knowledge of Good Clinical Practice, Institutional Review Board, Veterans Administration, and Food and Drug Administration regulations
Proficient experience in REDCap surveys and data entry (for Senior Level)
Related professional experience as manager, supervisor, work leader, staff authority or project/program administrator (for Senior Level)
Can juggle multiple projects without losing your attention to detail
Communicate clearly and confidently with participants, clinical staff, and research teams alike
Take personal accountability seriously and enjoy working with a high degree of independence in a fast-paced environment
Bring genuine curiosity to your work and care about the science behind what you're doing
Knowledge and understanding of federal regulations and Good Clinical Practice (GCP)
Ability to communicate effectively, both in writing and orally
Ability to establish and maintain effective working relationships with employees at all levels throughout the institution
Outstanding customer service skills
Ability to interpret and master complex research protocol information

Responsibilities

Serve as Coordinator on multiple human subject research studies, mastering protocols and study documents and ensuring every procedure meets regulatory standards
Drive participant recruitment — from pre-screening and phone contacts to in-person interviews and eligibility confirmation
Guide participants through the informed consent process and coordinate all scheduling logistics, including clinical resources such as nursing, laboratory, radiology, and pharmacy
Collect, code, and analyze study data with precision, maintaining records in compliance with FDA requirements, IRB standards, and applicable SOPs
Contribute to process improvement by supporting the development of SOPs and quality assurance initiatives that make the whole team better
Perform data entry and quality reviews in REDCap and Excel