Clinical Research Coordinator - Ophthalmology
$59,384–$86,112 year
On-site · Chicago, Illinois, United States
Job Summary
Coordinate all aspects of ophthalmology clinical trials under the Principal Investigator, ensuring adherence to Good Clinical Practice, SOPs, and sponsor requirements. Manages patient care and study visits, dispenses investigational medications as delegated, conducts data entry into CRFs with source documentation verification, documents adverse events, prepares for IRB submissions, and coordinates communications among subjects, investigators, sponsors, and study monitors. Requires a Bachelor’s degree and at least two years of clinical research experience with strong organizational, communication, and customer-service skills; travel between hospital locations is expected.
Required Qualifications
- Bachelor’s Degree in related field or equivalent experience in lieu of a degree
- Two years’ experience in managing all aspects of clinical research trials with in-depth knowledge of protocol requirements and Good Clinical Practice
- Intermediate computer and internet knowledge
- Excellent customer service and patient care skills
- Meticulous organizational skills
- Excellent demonstrated written and verbal communication abilities
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