Clinical Research Coordinator II — Flexible Hours

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

Benefits offered by this job

Benefits from Day One

Paid Time Off from Day One

403-B Retirement Plan

4 Weeks 100% Paid Parental Leave

Career Development

Whole Person Well-being Resources

Mental Health Resources and Support

Pet Benefits

Job summary

AdventHealth in Denver, CO is seeking a diligent Clinical Research Coordinator to oversee multiple clinical trial protocols, ensure accurate documentation, and uphold regulatory standards across studies. You will work with Principal Investigators, sponsors, and healthcare teams to maintain trial integrity and participant safety.

Applicants should have a Bachelor's degree, 2+ years in clinical research, and familiarity with FDA/ICH guidelines; bilingual English/Spanish is preferred.

Qualifications

• Bachelor's degree required.
• 2+ years of clinical research experience.
• Knowledge of FDA/ICH guidelines and related regulatory requirements.

Responsibilities

• Coordinate and manage multiple clinical trial protocols with accurate documentation.
• Oversee adherence to regulatory requirements and trial integrity.
• Collaborate with investigators, sponsors, and clinical staff.
• Assist with start-up, execution, modification, renewal, and termination of studies.
• Communicate with healthcare teams and participants; ensure informed consent.

Skills

Independent work

Interpersonal communication

Detail-oriented

Multitasking

Regulatory knowledge

Bilingual (English/Spanish)

Education

Bachelor's degree

Tools

Microsoft Office

Job description

AdventHealth in Denver, CO is seeking a diligent Clinical Research Coordinator to oversee multiple clinical trial protocols, ensure accurate documentation, and uphold regulatory standards across studies. You will work with Principal Investigators, sponsors, and healthcare teams to maintain trial integrity and participant safety.

Applicants should have a Bachelor's degree, 2+ years in clinical research, and familiarity with FDA/ICH guidelines; bilingual English/Spanish is preferred.