On-Site Senior Clinical Research Coordinator — Impact Lead

UIC

Chicago, Northern (IL, KY)

Hybrid

USD 70,000 - 90,000

Full time

13 days ago

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Job summary

University of Illinois Chicago in Chicago, IL seeks a Visiting Senior Clinical Research Coordinator to support the Department of Medicine's Breathe Chicago Center. The role manages multi-study operations, from startup through close-out, serving as a liaison with physicians, nurses, data staff and sponsors.

Eligible candidates will have a bachelor’s degree in a related field and at least five years of human participant research experience (or three years plus a master’s).

Qualifications

  • Bachelor’s degree in a relevant field is required.
  • Five years of experience conducting human participant research, or three years plus a master’s degree.
  • Experience in a clinical research setting with Federal Regulations and IRBs is required.
  • Strong communication, writing, presentation, and interpersonal skills are essential.

Responsibilities

  • Oversee and manage goals and tasks per the project plan to meet milestones.
  • Develop, update, and execute MOPs and SOPs; train study staff on protocols.
  • Coordinate participant treatment schedules and visits to stay within protocol windows.
  • Ensure accurate data entry and regular data audits and reporting.
  • Mentor junior staff and present study progress internally or at conferences.

Skills

Communication skills
Team coordination
Leadership
Multitasking

Education

Bachelor's degree in nursing, mental health, psychology, pharmaceutical sciences, social science, or related field

Tools

EMR systems
IRB processes

Job description

University of Illinois Chicago in Chicago, IL seeks a Visiting Senior Clinical Research Coordinator to support the Department of Medicine's Breathe Chicago Center. The role manages multi-study operations, from startup through close-out, serving as a liaison with physicians, nurses, data staff and sponsors.

Eligible candidates will have a bachelor’s degree in a related field and at least five years of human participant research experience (or three years plus a master’s).

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