Research Services Intermediate Professional

University of Colorado•Aurora, CO

20h•Onsite

About The Position

The B4 Health Lab is looking for a sharp, curious, and driven researcher to join our team full-time. Our work sits at the intersection of the Brain, Body, Biome, and Behavior — exploring how these systems connect to advance both physical and mental health. This is not a passive support role. You'll be a primary coordinator across multiple active studies, with real ownership over how research gets done.

Requirements

Bachelor's degree in a related field (or equivalent professional experience, year for year)
At least one year of human clinical research administration experience, including familiarity with research methods, protocols, data collection, and analysis
U.S. Citizenship or Permanent Resident status (required due to funding restrictions)
Ability to perform duties with minimal guidance and direction from other professionals.
Ability to interpret and master complex research protocol information.
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.
Demonstrated commitment to providing outstanding customer service skills.
Knowledge of basic human anatomy, physiology, and medical terminology.
Understanding and adherence to SOPs, Good Clinical Practice (GCP), IRB, VA, and FDA regulations.
Experience in ensuring all regulatory procedures are completed accurately and on time.
Attention to detail to maintain compliance with all regulatory standards.
Ability to manage multiple individual research projects concurrently while maintaining regulatory compliance.
Skills in planning, scheduling, and resource allocation to meet project milestones and goals.
Experience in maintaining accurate and comprehensive documentation for all studies.
Attention to detail in record-keeping to ensure compliance with regulatory standards.
Skills in developing and maintaining standard operating procedures (SOPs).

Nice To Haves

Master’s degree in science or health related field
Experience in REDCap surveys and data entry
Strong working knowledge of GCP, IRB, VA, and FDA regulations
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

Responsibilities

Serve as Primary Coordinator on multiple 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