Clinical Research Coordinator - Aurora, CO

IQVIA • SD

94d • $35 - $42

About The Position

The Clinical Research Coordinator will be responsible for coordinating clinical research studies under the supervision of a principal investigator. This role requires performing complex clinical procedures, including phlebotomy, ECG, sample collection, and vital signs monitoring. The coordinator will also engage in community outreach and ensure the well-being of study subjects while maintaining high standards of safety and care. Responsibilities include updating skills and knowledge of best practices, addressing volunteer concerns, and supporting study conduct through various logistical and administrative tasks.

Requirements

• High School Diploma and 1 year of relevant work experience in clinical research.
• At least 1 year of experience working in a clinical research setting preferred.
• Applicable certifications and licenses as required by regulatory bodies.
• Working knowledge of clinical trials and Good Clinical Practices (GCP).
• In-depth knowledge of protocol and study-specific operating procedures.
• Skill in carrying out required clinical procedures.
• Working knowledge of medical terminology.
• Ability to pay close attention to detail.
• Ability to establish and maintain effective working relationships.

Responsibilities

• Perform phlebotomy and other complex clinical procedures on subjects.
• Coordinate clinical research studies conducted by a supervising principal investigator.
• Update and maintain skills, training, and knowledge of current best nursing practices.
• Safeguard the well-being of the subjects and maintain high standards.
• Act as a volunteer advocate and address concerns proactively.
• Assist staff in clinical coordinator practices and delivery of care.
• Review study protocols and participate in project meetings.
• Perform clinical set-up and preparation for studies.
• Generate volunteer instructions and prepare study-specific training materials.
• Recruit and screen volunteers for inclusion in studies.
• Orient volunteers to the study and the site.
• Collect, record, and report clinical data appropriately.
• Collaborate with the study investigator on adverse events.
• Follow ICH GCP guidelines regarding study and patient activities.

Benefits

• Potential base pay range of $35.00-$42.00 per hour.
• Incentive plans, bonuses, and/or other forms of compensation may be offered.
• Health and welfare benefits.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED
• Number of Employees: 5,001-10,000 employees