Clinical Research Coordinator II: Trials & Compliance

AdventHealth; Parker (CO); On-site; USD 57,000 - 105,000; Full time

Benefits offered by this job

Medical, Dental, Vision Insurance

Life Insurance

Disability Insurance

403-B Retirement Plan

Paid Parental Leave

Career Development

Well-being Resources

Mental Health Resources

Pet Benefits

Job summary

AdventHealth in Denver, CO is seeking a detail-focused Clinical Research Coordinator to manage multiple protocols, coordinate execution, and ensure accurate documentation in clinical trials.

You will collaborate with Principal Investigators, IRB, and study sponsors, review consent forms, and maintain regulatory compliance while supporting patient advocacy and data integrity. This role requires strong communication, organization, and ability to work under pressure.

Qualifications

• Bachelor's degree required.
• 2+ clinical research experience required.
• Experience with FDA/OHRP/ICH/GCP guidelines required.
• Strong documentation and regulatory skills.
• Ability to coordinate diverse clinical trials and communicate with teams.

Responsibilities

• Coordinate and manage multiple clinical trial protocols.
• Promote trial integrity and regulatory compliance.
• Review informed consent documents and ensure patient advocacy.
• Liaise with Principal Investigators, IRB, and sponsors.
• Prepare study start-up, execution, renewal and termination docs.

Skills

Independent work

Interpersonal skills

Detail-oriented

Multi-tasking

Regulatory knowledge

Critical thinking

Microsoft Office

Clinical study coordination

FDA/CDC/HHS knowledge

Bilingual English/Spanish (preferred)

Education

Bachelor's degree

Tools

Microsoft Office

Job description

AdventHealth in Denver, CO is seeking a detail-focused Clinical Research Coordinator to manage multiple protocols, coordinate execution, and ensure accurate documentation in clinical trials.

You will collaborate with Principal Investigators, IRB, and study sponsors, review consent forms, and maintain regulatory compliance while supporting patient advocacy and data integrity. This role requires strong communication, organization, and ability to work under pressure.