Clinical Research Coordinator: Study Operations & Compliance

Cook County; Bayshore (FL); On-site; USD 52,000 - 78,000; Full time

Benefits offered by this job

Medical, dental, and vision coverage

Retirement plan and PSLF eligibility

Paid holidays, vacation, and sick time

Professional development opportunities

Job summary

Cook County Health & Hospitals System in Florida seeks a Clinical Research Coordinator to assist with recruitment, screening and consent, and to support study conduct throughout the lifecycle, ensuring adherence to GCP and sponsor guidelines. The role requires an associate degree and 2 years of clinical research experience; bachelor’s degree is preferred.

Strong documentation and communication skills, with knowledge of regulatory requirements, are essential for success.

Qualifications

• Associate degree from an accredited college or university or higher.
• Two (2) years in a clinical research or relevant experience.
• Proficiency using Microsoft Office (Excel and Word).
• Knowledge of GCP concepts and human subject research regulations.

Responsibilities

• Maintains accurate and timely documentation and communicates with investigators, study participants, sponsors, IRB, and related entities.
• Ensures study procedures are executed per protocol and timelines.
• Participates in study recruitment including screening and consent of eligible participants.
• Obtains consent and ensures participants understand the protocol.
• Identifies adverse events and reports them to investigators and regulatory authorities.

Skills

Attention to detail

Communication

Confidentiality

Clinical research knowledge

Education

Associate degree

Bachelor’s degree preferred

Tools

MS Office (Excel, Word)

Job description

Cook County Health & Hospitals System in Florida seeks a Clinical Research Coordinator to assist with recruitment, screening and consent, and to support study conduct throughout the lifecycle, ensuring adherence to GCP and sponsor guidelines. The role requires an associate degree and 2 years of clinical research experience; bachelor’s degree is preferred.

Strong documentation and communication skills, with knowledge of regulatory requirements, are essential for success.