Clinical Research Coordinator (Open Rank, Intermediate or Senior)

University of Colorado•Aurora, CO

1d•Onsite

About The Position

As a Clinical Research Coordinator in the Yomogida Lab at the University of Colorado Anschutz Medical Campus, you will play a key role in advancing groundbreaking research in immunology and pediatric autoimmune diseases. This position provides a unique opportunity to contribute directly to impactful biomedical research while developing strong hands-on laboratory and clinical research skills. In this role, you will communicate with patients and families to obtain informed consent for research participation and will be responsible for processing and storing clinical specimens according to established protocols. The position combines patient interaction with laboratory-based responsibilities, offering an ideal training environment for individuals interested in translational science, immunology, or future careers in medicine, graduate school, or industry research.

Requirements

Bachelor’s degree in any field.
A combination of education and related technical/paraprofessional experience may be substituted for the bachelor’s degree on a year for year basis.
One (1) year clinical research or related experience.
An advanced degree (Masters or Doctorate) may be substituted for experience on a year for year basis if the degree is in a field of study directly related to the work assignment.
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.
Knowledge of basic human anatomy, physiology, and medical terminology.
Ability to interpret and master complex research protocol information.
Ability to interact professionally with patients, families, and clinical staff.
Competence in reviewing and abstracting patient information from electronic medical records (EPIC).
Ability to perform basic wet laboratory techniques, including pipetting, centrifugation, biospecimen handling, sterile technique, and sample processing.
Strong organizational and time-management skills, with the ability to prioritize tasks and in a fast-paced clinical research environment.
Ability to follow detailed standard operating procedures (SOPs) and maintain accurate documentation.
Demonstrated reliability and professionalism.
Attention to detail and commitment to accurate documentation and adherence to standard operating procedures (SOPs).
Ability to maintain confidentiality and comply with HIPAA, biosafety, and institutional research regulations.

Nice To Haves

Master’s degree in biology, public health, molecular biology, clinical research, chemistry, biomedical sciences, genetics, or related field
Experience in clinical research, participant recruitment, informed consent, or clinical trial coordination.
Experience communicating with patients and families in a healthcare or research setting.
Hands-on experience with wet laboratory procedures such as sample processing, tissue handling, or basic molecular techniques.
Two (2) years or more years of experience in an experimental or wet laboratory.
Familiarity with REDCap, EPIC, or other clinical data management systems.

Responsibilities

Identify eligible research participants and clearly explain study procedures to patients and families.
Obtain informed consent/assent in accordance with IRB-approved protocols and institutional policies.
Coordinate and assist with specimen collection during clinic visits and procedures.
Process, label, and aliquot clinical biospecimens (blood, synovial fluid, and tissue) following established SOPs.
Ensure proper storage and tracking of samples in liquid nitrogen, −80°C freezers, or other designated storage systems.
Maintain accurate documentation in electronic lab notebooks, REDCap, and other data management systems.
Perform basic wet-laboratory tasks, including pipetting, centrifugation, sterile technique, and preparation of reagents.
Monitor and organize laboratory inventory, including ordering supplies and maintaining stock levels.
Support lab operations by helping schedule meetings, maintain shared workspaces, and ensure regulatory compliance.
Communicate effectively with clinical teams, study personnel, and other collaborators to ensure smooth workflow.