Clinical Research Coordinator

University Retina•Lemont, IL

6d•$25 - $29•Onsite

About The Position

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 actively recruiting for a Clinical Research Coordinator to join our growing team at University Retina and Macula Associates. A Clinical Research Coordinator (CRC) is responsible for performing procedures and coordinating the execution of clinical trials in accordance with research protocols. If you wish to join a growing team with favorable benefits and perks, while contributing to a best-in-class organization, please apply with your resume.

Requirements

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

Responsibilities

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)