Clinical Research Assistant: Critical Care & Pulmonary(PT)

Lurie Children's; Chicago (IL); On-site; USD 27,000 - 42,000; Part time

Job summary

Ann & Robert H. Lurie Children’s Hospital of Chicago is seeking a part-time Clinical Research Assistant for Critical Care Medicine and Pulmonary Medicine in Chicago's River North area.

The role supports investigators, coordinates visits, and maintains regulatory documents to ensure ethical and compliant conduct of pediatric clinical research. Responsibilities include data collection, specimen handling, and assisting in site visits by sponsors or regulators.

Qualifications

• High School diploma required.
• Bachelor’s degree and experience and/or training in research preferred.
• Good organizational skills.
• Good verbal and written communications skills.
• Some knowledge of FDA, HSR, and GCP Guidelines.
• Some analytical skills with the ability to remain agile and adaptable to various technological systems.

Responsibilities

• Assists investigators and study team in the implementation, coordination, and conduct of clinical research activities.
• Assist with study start-up and maintain regulatory documents required by sponsors and regulatory agencies.
• Assist in scheduling study visits according to protocol, in coordination with the PI and study team, and research support services.
• Prepares necessary supplies for study visits (consent forms, data collection materials, lab kits, etc.).
• Assists in the collection of data and/or specimens from research participants and/or medical records, as authorized.
• Supports data entry and maintains/updates databases as needed.

Skills

Organizational skills

Verbal and written communication

FDA/HSR/GCP knowledge

Analytical skills

Education

Bachelor’s degree in research

High School diploma

Job description

Ann & Robert H. Lurie Children’s Hospital of Chicago is seeking a part-time Clinical Research Assistant for Critical Care Medicine and Pulmonary Medicine in Chicago's River North area.

The role supports investigators, coordinates visits, and maintains regulatory documents to ensure ethical and compliant conduct of pediatric clinical research. Responsibilities include data collection, specimen handling, and assisting in site visits by sponsors or regulators.