Neurology Clinical Research Coordinator II - Lead Trials

uchicago; Chicago (IL); On-site; USD 60,000 - 75,000; Full time

Job summary

The University of Chicago Medical Center is seeking a Clinical Research Coordinator II (CRC II) to work onsite with the Principal Investigator and Clinical Research Manager, coordinating daily clinical trial activities and ensuring protocol adherence.

You will screen and enroll subjects, obtain informed consent, collect data, manage visit schedules, and maintain regulatory documentation while protecting patient confidentiality and data security.

Qualifications

• Requires a college or university degree in a related field.
• 2–5 years of work experience in a related job discipline.
• Familiarity with Good Clinical Practices (GCP) and regulatory requirements.

Responsibilities

• Manages all aspects of conducting clinical trials including screening, enrollment, subject follow-up, case report forms, and adverse event reports.
• Coordinates study startup through closeout including recruitment, informed consent, data collection, protocol adherence, and data integrity.
• Recruits and interviews potential study patients with guidance from PI and staff.
• Obtains informed consent.
• Plans and coordinates patient schedules for procedures, visits, and treatment schedules.
• Performs assessments at visits and monitors adverse events.
• Attends site visits with sponsors and study meetings.
• Protects patient data confidentiality and ensures compliance with regulations and sponsor protocols.
• Ensures SOPs are followed and documented per sponsor, PI, and regulatory specs.
• Maintains complete records including consent, IRB approvals, CRFs, and study communications.
• Manages IRB submissions and timely study initiation.

Skills

Strong communication

Interpersonal skills

Adaptability

Attention to detail

Multitasking

Time management

Training others

GCP knowledge

Education

Bachelor's degree

Related field degree

Job description

The University of Chicago Medical Center is seeking a Clinical Research Coordinator II (CRC II) to work onsite with the Principal Investigator and Clinical Research Manager, coordinating daily clinical trial activities and ensuring protocol adherence.

You will screen and enroll subjects, obtain informed consent, collect data, manage visit schedules, and maintain regulatory documentation while protecting patient confidentiality and data security.