Open-Rank Clinical Research Coordinator – Pain Trials

University of Colorado

Aurora (CO)

On-site

USD 54,302 - 72,765

Full time

14 days+
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Benefits offered by this job

Medical: Multiple plan options
Dental: Multiple plan options
401(a) Plan: Employer contributes 10%
Paid Time Off: 22 vacation days/year
Sick Days: 15/year
Tuition Benefit available
ECO Pass: Reduced rate RTD Bus service

Job summary

The University of Colorado is seeking a Clinical Research Coordinator for the Emily Lindley Research Lab. The successful candidate will assist with studies on non-opioid alternatives for chronic pain and may be hired at either the intermediate or senior level.

Responsibilities include overseeing clinical trials, performing informed consent processes, and collecting data. Applicants should possess a Bachelor's degree and relevant clinical research experience. Comprehensive benefits package is provided.

Qualifications

  • 1 year of clinical research or related experience for intermediate level.
  • 2 years of clinical research or related experience for senior level.
  • Ability to establish and maintain effective working relationships.

Responsibilities

  • Assist with and oversee day-to-day operations of clinical trials.
  • Perform the informed consent process ensuring compliance.
  • Collect, code, and analyze data from research studies.

Skills

Knowledge of federal regulations and Good Clinical Practice (GCP)
Effective communication skills
Customer service skills
Understanding of human anatomy and physiology

Education

Bachelor's degree in any field
Bachelor's degree in science or health-related field preferred

Tools

Electronic data capture systems experience

Job description

The University of Colorado is seeking a Clinical Research Coordinator for the Emily Lindley Research Lab. The successful candidate will assist with studies on non-opioid alternatives for chronic pain and may be hired at either the intermediate or senior level.

Responsibilities include overseeing clinical trials, performing informed consent processes, and collecting data. Applicants should possess a Bachelor's degree and relevant clinical research experience. Comprehensive benefits package is provided.

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