Onsite Oncology Trials Coordinator - Lead Protocols
Listed on 2026-10-06
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Science
Clinical Research
Advocate Health is seeking an onsite Research Coordinator to coordinate clinical trials and related studies. You will guide physicians, staff, and sponsors, ensuring adherence to protocols and regulatory requirements across sites.
The role requires 2 years of research experience and a strong background in GCP/ICH, with proficiency in EMR and MS Office. Collaboration with investigators and a commitment to quality and patient safety are essential.
As a Onsite Oncology Trials Coordinator
- Lead Protocols, you will play an important part at Advocate Health in Crystal Lake, IL, United States.
We appreciate your interest in this position.
Join Advocate Health and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the Onsite Oncology Trials Coordinator
- Lead Protocols role at Advocate Health, based in Crystal Lake, IL, United States.
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