1

Ophthalmology Clinical Research Jobs (NOW HIRING)

Clinical Research Assistant

Lemont, IL · On-site

$21 - $23.50/hr

Led by a team of board-certified ophthalmologists and retina specialists, the practice has ... Position Summary We are now hiring for a Clinical Research Assistant that will support a high ...

Clinical Research Assistant

Lemont, IL · On-site

$21 - $23.50/hr

Led by a team of board-certified ophthalmologists and retina specialists, the practice has ... Position Summary We are now hiring for a Clinical Research Assistant that will support a high ...

Showing results 41-60

Ophthalmology Clinical Research information

See salary details

$13

$24

$40

How much do ophthalmology clinical research jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for ophthalmology clinical research in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What is an ophthalmology clinical research job?

An Ophthalmology Clinical Research job involves conducting studies to evaluate new treatments, drugs, or medical devices related to eye health. Professionals in this field work with patients, collect and analyze data, and ensure compliance with regulatory guidelines. They collaborate with physicians, scientists, and clinical trial teams to advance eye care and improve patient outcomes. This role may include managing clinical trials, recruiting participants, and reporting results. It requires knowledge of ophthalmic conditions, research methodologies, and ethical standards in human studies.

What are the typical daily responsibilities of someone working in ophthalmology clinical research?

Daily responsibilities in Ophthalmology Clinical Research often include coordinating patient recruitment and consent, collecting and managing clinical data, and ensuring all study procedures adhere to regulatory guidelines. You may also assist with ophthalmic examinations, imaging, and documentation, as well as liaise with study sponsors, physicians, and regulatory bodies. Keeping meticulous records and monitoring study participants’ progress are key parts of the job. This role requires constant collaboration with both clinical and research teams to ensure seamless study operations and quality results.

What are the key skills and qualifications needed to thrive in ophthalmology clinical research?

To thrive in Ophthalmology Clinical Research, you need knowledge of clinical trial protocols, ophthalmic terminology, and data management, typically supported by a degree in a medical or life sciences field. Familiarity with electronic data capture systems (EDC), Good Clinical Practice (GCP) certification, and imaging modalities such as OCT is highly valuable. Attention to detail, strong organizational skills, and effective communication are standout soft skills in this role. These competencies are essential for conducting accurate research, maintaining regulatory compliance, and ensuring the integrity and success of ophthalmic studies.

More about Ophthalmology Clinical Research jobs

What cities are hiring for Ophthalmology Clinical Research jobs?

Cities with the most Ophthalmology Clinical Research job openings:

What are the most commonly searched types of Ophthalmology Clinical Research jobs?

The most popular types of Ophthalmology Clinical Research jobs are:

What states have the most Ophthalmology Clinical Research jobs?

States with the most job openings for Ophthalmology Clinical Research jobs include:

Infographic showing various Ophthalmology Clinical Research job openings in the United States as of August 2026, with employment types broken down into 78% Full Time, 11% Part Time, and 11% Temporary. Highlights an 100% In-person job distribution, with an average salary of $50,108 per year, or $24.1 per hour.

Clinical Research Coordinator

Visionary Eye Institute Inc

Newport Beach, CA • On-site

$26 - $34.50/hr

Full-time

Medical, Dental, Vision, Life

Re-posted 18 days ago


Job description

Are you interested in working in clinical research? Do you have a background in nursing or life sciences and are interested in bringing innovation to your community? Do you want to use your strong organizational skills to help others? If so, a position as a clinical research coordinator might be the fit for you. Clinical Research Coordinators conducting studies in a private, ophthalmology practice is a position that allows ongoing growth and development.  As an clinical research coordinator, you’ll assist principal investigators in recruiting and management research studies directly affecting the eyecare industry. Join Visionary Eye Institute to grow in this exciting position and start your new career!
Visionary Eye Institute was founded by Dr. Ehsan Sadri in 2019 to advocate for all communities by providing innovative and life-changing eyecare. Our practice specializes in medical eyecare and surgery, and we also have a clinical research division that allows us to offer the highest-level care to Los Angeles and Orange County.  We have excellent benefits including paid holiday, and medical/dental benefits. Come join our caring and professional team today!
 
EDUCATION AND EXPERIENCE:

1.     Bachelor’s degree in nursing or life sciences.
2.     3+ years’ work experience for a pharmaceutical company or related field
3.     Experience as an ophthalmic technician preferred but not required.
 

ESSENTIAL SKILLS AND ABILITIES:

1.     Proficient understanding of marketing and statistics.
2.     Outstanding communication skills, both verbal and written.
3.     Proficient with Microsoft Office Word and Excel.
4.     Ability to work independently and prioritize duties.
5.     Understanding of electronic data capture.
6.     Strong organization with attention to detail.
7.     Analytical problem-solving skills.
8.     Demonstrated ability to meet deadlines.
 
KEY RESPONSIBILITIES:

1.     Develops and outlines trial protocols.
2.     Develops and maintains site certification for ongoing studies.
3.     Trains clinical research staff on protocol requirements, proper source documentation, and case report form completion.
4.     Works with the physicians on ethics regarding rights, safety, and well-being of trial subjects.
5.     Develops protocols to protect subjects’ confidentiality.
6.     Manages all trial materials.