Clinical Research Coordinator: Compliance, Coordination, Impact

HSHS Medical Group; Springfield (IL); On-site; USD 30,307 - 45,460; Full time

Benefits offered by this job

Health coverage

PTO

Education assistance

Job summary

Hospital Sisters Health System seeks a Clinical Research Specialist to coordinate research activities across treatment sites and ensure quality and efficiency of clinical trials. You will support front line research staff and assure compliance with study protocols and regulatory requirements.

The role is based at Springfield - St. John's Hospital, with a Monday–Friday schedule, 8:00 AM–4:30 PM, and requires an associate degree in a science or healthcare field, two years in healthcare and

Qualifications

• Associate degree in science or healthcare required; bachelor’s degree preferred.
• Two years of healthcare experience; two years in research preferred.
• CITI training and human subject protection training required within 30 days of hire.

Responsibilities

• Coordinates research activities across treatment sites to maintain quality and promote efficiency.
• Ensures compliance with regulatory requirements for all study protocols.
• Assists front line research staff in all research study activities.

Skills

Regulatory compliance

Research coordination

CITI training

Education

Associate degree in science/healthcare

Bachelor's degree preferred

High school diploma + 3 years experience accepted

Job description

Hospital Sisters Health System seeks a Clinical Research Specialist to coordinate research activities across treatment sites and ensure quality and efficiency of clinical trials. You will support front line research staff and assure compliance with study protocols and regulatory requirements.

The role is based at Springfield - St. John's Hospital, with a Monday–Friday schedule, 8:00 AM–4:30 PM, and requires an associate degree in a science or healthcare field, two years in healthcare and