Clinical Research Coordinator - Trials, Data & Compliance

Ultipro; Englewood, Northern (CO, KY); Hybrid; USD 39,000 - 48,000; Full time

Job summary

CenExel Clinical Research is a leading nationwide clinical research site and patient network. We coordinate clinical trials with strict adherence to ICH, GCP, and sponsor guidelines, ensuring data integrity and patient safety across multiple centers.

As a Clinical Research Coordinator, you will support trial initiation, patient involvement, data collection, and regulatory documentation while collaborating with investigators, vendors, and sponsors to maintain high-quality study conduct.

Qualifications

• Bachelor's degree preferred; high school diploma acceptable.
• 0–3 years of experience in the medical field.
• Knowledge of Federal regulations protecting human subjects in research.
• Strong leadership and mentorship skills.
• Ability to communicate effectively verbally and in writing.

Responsibilities

• Coordinates all aspects of patient involvement from study initiation until study completion.
• Organizes research information for clinical trials.
• Observes subjects and assists with data analysis and reporting.
• Schedules the collection of data.
• Documents adverse events, protocol deviations, and other issues appropriately.
• Reports research data to maintain quality and compliance.
• Performs administrative and regulatory duties related to the study.
• Performs safety and efficacy assessments per protocol.

Skills

Leadership

Communication

Teamwork

Crisis management

Regulatory knowledge

Education

Bachelor's degree

High school diploma or equivalent

Job description

CenExel Clinical Research is a leading nationwide clinical research site and patient network. We coordinate clinical trials with strict adherence to ICH, GCP, and sponsor guidelines, ensuring data integrity and patient safety across multiple centers.

As a Clinical Research Coordinator, you will support trial initiation, patient involvement, data collection, and regulatory documentation while collaborating with investigators, vendors, and sponsors to maintain high-quality study conduct.