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Ophthalmology Clinical Research Jobs (NOW HIRING)

ProTouch Staffing

Ophthalmology Physician

El Centro, CA

$168.27 - $240.38/hr

Participate in clinical research or trials to contribute to advancements in the field of ophthalmology * Maintain accurate and confidential patient records in compliance with HIPAA regulations

Lexitas

Clinical Research Coordinator

Erie, PA · On-site

$22 - $26/hr

We can help facilitate studies, bring products to market, collaborate on ophthalmology-related ... The Clinical Research Coordinator serves as a central liaison between investigators, patients ...

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Ophthalmology Clinical Research information

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How much do ophthalmology clinical research jobs pay per hour?

As of Aug 6, 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:
What job categories do people searching Ophthalmology Clinical Research jobs look for? The top searched job categories for Ophthalmology Clinical Research jobs are:
Ophthalmology Clinical Research jobs near you
Infographic showing various Ophthalmology Clinical Research job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $50,108 per year, or $24.1 per hour.

Ophthalmology Clinical Research Coordinator

ICON Strategic Solutions

Johns Creek, GA • On-site

$22.50 - $30/hr

Other

Medical, Dental, Vision, Life, Retirement

This job post has expired today. Applications are no longer accepted.

Job description

As a Clinical Research Coordinator at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.


Shift: 10:30 AM – 7:00 PM, Monday to Friday (8 working hours with a 30-minute unpaid lunch break), with flexibility required. The role will include at least two Saturdays per month, with Saturday shifts scheduled from 8:00 AM – 4:00 PM. A weekday off will be provided in lieu of each Saturday worked.



What You Will Do:


Your role will involve delivering clinical coordination work to a high standard, working closely with your team and stakeholders.


Key responsibilities include:

  • Facilitating the coordination and execution of clinical research studies, including participant recruitment, enrollment, and follow-up activities.
  • Collaborating with principal investigators, study sponsors, and regulatory authorities to ensure compliance with study protocols, regulatory requirements, and ethical standards.
  • Collecting and maintaining accurate and complete clinical trial data, including documentation of adverse events, protocol deviations, and study outcomes.
  • Managing study-related documentation, including informed consent forms, case report forms, and regulatory submissions.
  • Providing support and guidance to study participants, including education, counseling, and assistance with study-related procedures.


Your Profile:


You will bring relevant clinical coordination experience, along with the following qualifications and skills.


Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field.
  • Previous experience working in clinical research or healthcare settings preferred.
  • Knowledge of clinical research regulations, including FDA/EMA regulations, ICH-GCP guidelines, and HIPAA requirements.
  • Strong organizational, communication, and interpersonal skills, with the ability to work effectively in a team environment.
  • Detail-oriented with the ability to manage multiple tasks and priorities simultaneously.


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways


Apply