Clinical Research Coordinator II - Flexible Hours & Impact

AdventHealth

Denver (CO)

On-site

USD 56,000 - 105,000

Full time

7 days ago
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Benefits offered by this job

Medical Insurance
Dental Insurance
Vision Insurance
Life Insurance
Disability Insurance
Paid Time Off
403-B Retirement Plan
Parental leave

Job summary

AdventHealth in Denver seeks a detail-oriented Clinical Research Coordinator to manage multiple trial protocols, coordinate execution, and ensure accurate documentation.

You will review informed consent, support patient advocacy, and liaise with investigators, IRB, and sponsors to maintain trial integrity and regulatory compliance.

Strong communication, organizational skills, and the ability to work under pressure are essential; bilingual English/Spanish preferred.

Qualifications

  • Ability to work independently in fast-paced clinical or research environments.
  • Interpersonal skills to interact with diverse healthcare teams and the public.
  • Detail-oriented with teamwork, organized, capable of multitasking under pressure.

Responsibilities

  • Manage multiple clinical trial protocols, coordinate execution and follow-up, and document accurately.
  • Review informed consent documents and ensure patient advocacy throughout the trial.
  • Coordinate staff, labs, and study teams; liaison between PIs, IRB, and office of Sponsored Programs.
  • Prepare and review start-up, execution, modification, renewal, and termination documentation.
  • Maintain knowledge of regulatory requirements and implement changes as needed.

Skills

Independent work
Interpersonal skills
Detail-oriented
Multi-tasking
Regulatory knowledge
Bilingual (English/Spanish)

Education

Bachelor's degree

Tools

Microsoft Office

Job description

AdventHealth in Denver seeks a detail-oriented Clinical Research Coordinator to manage multiple trial protocols, coordinate execution, and ensure accurate documentation.

You will review informed consent, support patient advocacy, and liaise with investigators, IRB, and sponsors to maintain trial integrity and regulatory compliance.

Strong communication, organizational skills, and the ability to work under pressure are essential; bilingual English/Spanish preferred.

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