Clinical Research Assistant for Retina Practice

University Retina is a full-service practice that specializes in helping patients heal eyesight-robbing diseases of the retina, vitreous, and macula. Led by a team of board-certified ophthalmologists and retina specialists, the practice has locations in Oak Forest, Bedford Park, Lemont, Lombard, and Lincolnwood, Illinois.

With a dedication to education, technology, charity, and compassionate care, the University Retina team strives to provide patients with the highest level of retinal care in the world. The physicians diagnose and treat retinal-related conditions, including macular degeneration, diabetic retinopathy, retinal detachment repair, and other disorders of the retina, vitreous, and macula.

All University Retina offices are equipped with state-of-the-art technology, and each patient’s treatment plan includes the most current and effective therapies or services available.

We are now hiring for a Clinical Research Assistant that will support a high-volume Resarch Department within an ophthalmic practice that focuses on providing quality and compassionate care to each patient needed complete eye care services. 

This position might be for you if you:

• Are looking for a CAREER in a growing field that provides a unique growth path.
• Would like the opportunity to work with one of the largest comprehensive Ophthalmology groups in the country.
• Are committed to learning and growing in an evolving field.
• Have an interest and passion for the medical field or science in general.
• Are looking for meaningful work and to make a difference in your community.
• Love helping others and excel at customer service.
• Thrive in a fast-paced, team environment.
• Have excellent attention to detail.

A CRA is responsible for performing procedures and coordinating the execution of clinical trials in accordance with research protocols.

• Recruit and screen subjects to participate in trials

• Coordinate patient visits and perform procedures related to research

• Collect accurate data obtained from research visits

• Monitor research participants to ensure adherence to study protocol

• Adhere to Good Clinical Practice (GCP) guidelines including regulatory and ethical standards

• Maintain relationships with site staff, study subjects, and sponsor delegates

• Perform other related duties as assigned by the Clinical Research Coordinator

• Maintain compliance with all research Standard Operating Procedures (SOPs)

Education and/or Work Experience Requirements:

• 2+ years in healthcare, preferably ophthalmology, but not necessarily in clinical research

• Analytical mindset

• Attention to detail

• Exceptional interpersonal skills

• Superior verbal and written communication skills

• Understanding of laboratory procedures and equipment

• Proficiency in MS Office – Word, Excel and Outlook

• High school diploma or equivalent GED