Clinical Research Coordinator

Job Overview

This Clinical Research Coordinator position is at the heart of moving medical science forward. You'll manage the day to day operations of clinical trials, ensuring everything runs smoothly and ethically from participant screening to data collection. It's a role where precision meets patient care, all within a setting in Aurora, CO that values rigorous scientific standards.

Duties & Responsibilities

• Screening and enrolling eligible participants, guiding them through the informed consent process with clarity and compassion.
• Collecting, documenting, and managing clinical trial data with impeccable accuracy to meet protocol and regulatory requirements.
• Coordinating patient visits, handling biological specimens, and maintaining detailed source documentation.
• Preparing for and facilitating monitoring visits and audits, addressing queries from sponsors or CROs promptly.
• Ensuring strict adherence to the study protocol, GCP guidelines, and all institutional policies.

Requirements

• A Bachelor's degree in life sciences, nursing, or a related field is typically required. CCRP or similar certification is a major plus.
• At least one year of hands on experience coordinating clinical trials in an academic hospital or private research setting.
• You need a solid grasp of Good Clinical Practice (GCP) and IRB submission processes. Familiarity with EDC systems like Medidata Rave or REDCap is essential.
• The job involves frequent interaction with patients and requires sustained focus on complex documentation. You'll be on your feet often during clinic days.

What It's Like In This Role

You'll work closely with principal investigators, research nurses, and data managers. Most days are split between clinic hours with participants and desk time for regulatory work and data entry. The environment is collaborative but demands a high degree of personal accountability. Expect a full time schedule where no two weeks are exactly alike; some are heavy on recruitment, others on audit prep or close out visits.

Why You'll Like This Opportunity

The role offers real variety; you might work on oncology studies one year and cardiology trials the next depending on the hiring institution. There's clear potential to grow into senior coordinator or project management positions. You're constantly learning new protocols and regulations, which keeps your skills sharp and highly transferable within the Aurora, CO area's growing research sector.

Schedule & Work Type

This is primarily a full time, onsite position based in Aurora, CO. Some hybrid flexibility for administrative tasks might be possible after onboarding, but direct patient interaction requires a consistent physical presence at the research site. Standard business hours apply, though occasional early starts or late finishes align with participant visit schedules.

How To Apply

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Disclaimer

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Equal Opportunity

The hiring employer provides equal employment opportunity to all qualified individuals without regard to race, color, religion, or any other protected status under applicable law.