On-Site Clinical Research Assistant — Chicago
Energy Jobline ZR
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Job summary
Cedar Crosse Research Center in Chicago, IL seeks a Clinical Research Assistant to support study teams across Phase I–IV trials. You will assist CRCs and Investigators by performing protocol-driven visits, collecting data, and maintaining trial documentation in an inspection-ready state.
The ideal candidate is detail-oriented, patient-focused, with at least 1 year in clinical, medical-office, or research settings, and comfortable with phlebotomy, vital signs, ECGs, and lab specimen handling.
Qualifications
- Must have/have access to healthcare or research setting experience.
- Familiarity with phlebotomy, vital signs, and ECG techniques.
- Strong attention to detail and documentation accuracy.
- Ability to work on-site full time, Monday–Friday.
- Desirable: EDC/CTMS/eSource experience and GCP training.
Responsibilities
- Welcome and support participants during study visits with professionalism.
- Perform protocol-required procedures and data collection per SOPs.
- Label, ship and manage lab specimens and inventory.
- Assist with pre-screening, scheduling, and retention activities.
- Document data accurately and support audits and monitoring.
- Maintain regulatory binders and study logs for inspections.
Skills
Education
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Job description
Cedar Crosse Research Center in Chicago, IL seeks a Clinical Research Assistant to support study teams across Phase I–IV trials. You will assist CRCs and Investigators by performing protocol-driven visits, collecting data, and maintaining trial documentation in an inspection-ready state.
The ideal candidate is detail-oriented, patient-focused, with at least 1 year in clinical, medical-office, or research settings, and comfortable with phlebotomy, vital signs, ECGs, and lab specimen handling.
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