Clinical Research Coordinator I: Data-Driven Trials

DM Clinical Research; Chicago (IL); On-site; USD 50,000 - 65,000; Full time

Job summary

A clinical research organization in Chicago is seeking a Clinical Research Coordinator I to ensure quality research is conducted at assigned sites according to protocols and regulations. The role involves conducting subject visits, documenting procedures, completing data entry, and collaborating with various teams to achieve study enrollment goals. Ideal candidates will have at least one year of CRC experience, with preferences for foreign medical graduates and ACRP certification.

Qualifications

• At least one year of experience as a CRC, preferably coordinating industry-sponsored vaccines.
• At least two years in a research assistant or related role in a clinical setting.
• ACRP or equivalent certification preferred.

Responsibilities

• Ensure quality research in accordance with sponsor protocols.
• Conduct study subject visits and document procedures.
• Complete data entry and resolve queries according to guidelines.
• Liaise with multiple teams for assigned protocols.
• Participate in subject recruitment and engagement efforts.

Skills

Detail-oriented

Multi-tasking

Goals-driven

Education

High School Diploma or equivalent

Foreign Medical Graduates preferred

Job description

A clinical research organization in Chicago is seeking a Clinical Research Coordinator I to ensure quality research is conducted at assigned sites according to protocols and regulations. The role involves conducting subject visits, documenting procedures, completing data entry, and collaborating with various teams to achieve study enrollment goals. Ideal candidates will have at least one year of CRC experience, with preferences for foreign medical graduates and ACRP certification.