Research Services Clinical Sciences Senior Professional (Onsite)
Job Summary
About the Role
The B4 Health Lab is seeking an experienced, self-directed clinical research professional to take a senior leadership role across multiple active studies. Our research explores the deep connections between the Brain, Body, Biome, and Behavior — translational work with real implications for physical and mental health. At the senior level, you won't just execute research; you'll shape how it gets done in our rigorous and rapidly advancing lab.
This is a role for someone who thrives with full ownership, brings seasoned regulatory instincts, and is ready to contribute not only to study operations but to the science itself in a dynamic, high-output research environment.
What You'll Do
As a Senior Clinical Sciences Professional, you'll operate independently across all phases of clinical research — from protocol mastery to publication support. Your core responsibilities will include:
- Leading project and trial coordination across multiple studies simultaneously, owning all protocols, SOPs, and regulatory documents end-to-end
- Driving participant recruitment and retention, including developing and implementing innovative strategies to maximize enrollment
- Conducting and documenting the full informed consent process, confirming eligibility, and obtaining comprehensive medical histories
- Managing all scheduling and study logistics, coordinating across physicians, nursing, laboratory, pharmacy, and other clinical resources
- Collecting, recording, and analyzing study data with precision, maintaining subject-level documentation, and reporting adverse events accurately and on time
- Developing and maintaining regulatory submissions, CRFs, process flows, and training materials in full compliance with FDA, hospital, and departmental standards
- Partnering with leadership to identify operational efficiencies and contributing directly to the presentation and publication of research findings
- Performing data entry and quality assurance reviews in REDCap and Excel
Work Location:
Onsite – this role is expected to work onsite five (5) days per week and is located in Aurora, CO.
Qualifications
Minimum Qualifications:
- Bachelor's degree in a related field (or equivalent professional experience, year for year)
- At least two (2) years of clinical research administration experience, with solid working knowledge of research methods, protocols, data collection, and analysis
- U.S. Citizenship or Permanent Resident status (required due to funding restrictions)
Preferred Qualifications:
- Master's degree in a science or health-related field
- Four (4) or more years of research administration experience
- Proficiency in REDCap
- Experience in a supervisory, project leadership, or staff authority capacity
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