Clinical Research Coordinator II — Lead Trials

AdventHealth; Denver (CO); On-site; USD 56,000 - 105,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

Paid Time Off

403B Retirement Plan

Parental Leave

Career Development

Well-being Resources

Mental Health Resources

Pet Benefits

Job summary

AdventHealth in Denver, CO is seeking an experienced Clinical Research Coordinator to oversee multiple trial protocols, ensure regulatory compliance, and coordinate cross-functional teams. You will work with Principal Investigators, IRB, and sponsors to maintain trial integrity while managing documentation and start-up activities.

The role demands 2+ years in clinical research, familiarity with FDA/OHRP/ICH/GCP guidelines, and strong organizational skills.

Qualifications

• Bachelor's degree required and 2+ years of clinical research experience.
• Experience with FDA/OHRP/ICH/GCP guidelines and regulatory standards.
• Familiarity with cardiology research is preferred.
• CCRC, BLS, ACLS are preferred certifications.

Responsibilities

• Manage multiple clinical trial protocols and documentation.
• Coordinate execution and follow-up, ensuring trial integrity.
• Advise on deviations and patient status with PI oversight.
• Liaise between Principal Investigators, IRB, and S.O.P. offices.
• Prepare study start-up, execution, modification, renewal and termination docs.
• Collaborate with sponsors and site monitors; support regulatory compliance.
• Maintain up-to-date regulatory knowledge and be flexible with hours.

Skills

Independent work

Interpersonal skills

Detail-oriented

Multitasking

Clinical trial coordination

Regulatory knowledge

Bilingual English/Spanish

Education

Bachelor's degree

Tools

Microsoft Office

Job description

AdventHealth in Denver, CO is seeking an experienced Clinical Research Coordinator to oversee multiple trial protocols, ensure regulatory compliance, and coordinate cross-functional teams. You will work with Principal Investigators, IRB, and sponsors to maintain trial integrity while managing documentation and start-up activities.

The role demands 2+ years in clinical research, familiarity with FDA/OHRP/ICH/GCP guidelines, and strong organizational skills.