Seeking a Clinical Research Coordinator to support Oncology Trials
Great opportunity that offers hybrid flexibility*
Job Description
Seeking a seasoned Clinical Research Coordinator to manage and oversee clinical research projects. Responsibilities include study start-up activities, maintaining regulatory documents, preparing protocols and consent documents, coordinating study conduct across departments, and recruiting eligible study subjects.
The coordinator will also handle site qualifications, study visits, data abstraction, specimen collection, and adverse event monitoring.
Additionally, the role involves preparing for audits, managing budgets, training personnel, and ensuring compliance with institutional and federal regulations.
Skill Requirements
- 3 years of Clinical Research Coordinating Experience
- Regulatory Experience with IRB Submittals and amendments
- Report writing
- Query updates
- Oncology Experience
Job Type
This is a Contract-to-Hire position with a duration of 6 Month(s).
Work Site
This is a hybrid position requiring some days on-site in Chicago, Illinois and some days remote.
Work Environment
Office setting, standard hours from 8 AM to 4 : 30 PM, Monday to Friday.
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