Clinical Research Assistant

EyeSouth Partners•Lemont, IL

12d•$21 - $24

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, and Lombard, 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. Position Summary 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. Pay Range - $21.00-$23.50/hr. Commensurate with 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

Responsibilities

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)