Clinical Research Coordinator I: Emergency Medicine Trials

The University of Chicago; Chicago (IL); On-site; USD 50,000 - 65,000; Full time

Job summary

The University of Chicago Medicine BSD MED Emergency Medicine is seeking a Clinical Research Coordinator 1 (CRC1) to support the PI and study team in daily trial activities, from startup through closeout, ensuring compliance and data integrity across study visits, consent, and regulatory documentation.

The role involves coordinating recruitment, screening, data collection, adverse event reporting, specimen handling, and site communications, with emphasis on protocol adherence and

Qualifications

• Minimum requirements include a college or university degree in related field.
• Minimum requirements include knowledge and skills developed through < 2 years of work experience in a related job discipline.
• Certifications: ---

Responsibilities

• Coordinate the conduct of the study from startup through closeout including recruitment and screening of study subjects, obtaining informed consent, collecting research data, and ensuring protocol adherence.
• Manages all aspects of conducting clinical trials including: screening, enrollment, subject follow-up, completion of the case report form, and adverse event reports.
• Recruit and interview potential study patients with guidance from PI and manager.
• Collect, process, ship and store specimens to appropriate laboratory according to established aseptic techniques.

Skills

Communication skills

Organizational skills

Interpersonal skills

Data management

MS Office

Education

Bachelor's degree

College degree in related field

Tools

Microsoft Word

Excel

Adobe Acrobat

Job description

The University of Chicago Medicine BSD MED Emergency Medicine is seeking a Clinical Research Coordinator 1 (CRC1) to support the PI and study team in daily trial activities, from startup through closeout, ensuring compliance and data integrity across study visits, consent, and regulatory documentation.

The role involves coordinating recruitment, screening, data collection, adverse event reporting, specimen handling, and site communications, with emphasis on protocol adherence and