Dynamic Clinical Research Coordinator II - Trials Oversight

adventhealth; Colorado; On-site; USD 56,000 - 105,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

PTO Day One

403-B Retirement

Job summary

AdventHealth in Denver, Colorado is seeking a Clinical Research Coordinator to manage multiple trial protocols, coordinate execution and documentation, and ensure regulatory compliance under PI oversight. You will collaborate with investigators, the IRB, and office of sponsored programs to maintain trial integrity and patient advocacy.

The role requires a Bachelor's degree, 2–5 years of clinical research experience, familiarity with FDA/ICH guidelines, and proficiency with Microsoft Office.

Qualifications

• Bachelor's degree required.
• 2+ years of clinical research experience.
• Familiarity with FDA, OHRP, ICH, and GCP guidelines.

Responsibilities

• Manages multiple clinical trial protocols and coordinates execution.
• Promotes PI oversight by advising on deviations and trial integrity issues.
• Reviews informed consent documents and ensures patient advocacy throughout the trial.
• Coordinates staff, laboratory technicians, and assistants for efficient results.
• Prepares and reviews documentation for study start-up, execution, modification, renewal and termination.

Skills

Independent work

Interpersonal skills

Detail-oriented

Multi-tasking

Clinical trials coordination

FDA/ICH familiarity

Bilingual English/Spanish

Education

Bachelor's degree

Tools

Microsoft Office

Job description

AdventHealth in Denver, Colorado is seeking a Clinical Research Coordinator to manage multiple trial protocols, coordinate execution and documentation, and ensure regulatory compliance under PI oversight. You will collaborate with investigators, the IRB, and office of sponsored programs to maintain trial integrity and patient advocacy.

The role requires a Bachelor's degree, 2–5 years of clinical research experience, familiarity with FDA/ICH guidelines, and proficiency with Microsoft Office.