Pediatric Clinical Research Coordinator II Multi-Site Trials

The University of Chicago; Chicago (IL); On-site; USD 60,000 - 75,000; Full time

Job summary

The University of Chicago seeks a Clinical Research Coordinator 2 (CRC2) in Pediatrics to provide research support under the supervision of the Director of Clinical Research and study team. The CRC2 will participate in multi-center trials, industry-supported studies, and disease-specific sections, handling data collection and regulatory processes.

The role requires robust data management, knowledge of GCP, and experience coordinating various study types.

Qualifications

• Education: Minimum requirements include a college or university degree in related field.
• Work Experience: Minimum requirements include knowledge and skills developed through 2-5 years of work experience in a related job discipline.
• Certifications:---

Responsibilities

• Ensures SOPs are implemented and documented in accordance to sponsor, PI, and regulatory specifications.
• Coordinates and may participate in quality assurance reviews, including site visits and audits.
• Understands the IRB submission and review process and facilitates study initiation through IRB submissions.
• Collects, processes, ships and stores specimens per aseptic techniques.
• Prepares program conference lists for multidisciplinary conferences and workshops.
• May assist in training of new or backup coordinators.
• Accounts for all tasks in moderately complex clinical studies.
• Assists with various professional, organizational, and operational tasks under moderate supervision.
• Facilitates daily activities of moderately complex clinical studies and performs data retrieval and documentation.

Skills

Data management

Attention to detail

Medical terminology

GCP knowledge

MS Word

Excel

Adobe Acrobat

Regulatory knowledge

Education

Bachelor's degree

Job description

The University of Chicago seeks a Clinical Research Coordinator 2 (CRC2) in Pediatrics to provide research support under the supervision of the Director of Clinical Research and study team. The CRC2 will participate in multi-center trials, industry-supported studies, and disease-specific sections, handling data collection and regulatory processes.

The role requires robust data management, knowledge of GCP, and experience coordinating various study types.