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Ophthalmology Cra Jobs (NOW HIRING)

Fortrea

FSP - Sr. CRAs & CRA 1/2 - Ophthalmology

OR · On-site +1

$110 - $145K/hr

Seeking Sr. CRA level and CRA 1s and 2s (1-2 years of monitoring). WHAT YOU WILL DO You will ... Ophthalmology experience is required * 60-70% overnight travel The important thing for us is you ...

Fortrea

FSP - Sr. CRAs & CRA 1/2 - Ophthalmology

$110 - $145K/hr

Seeking Sr. CRA level and CRA 1s and 2s (1-2 years of monitoring). WHAT YOU WILL DO You will ... Ophthalmology experience is required * 60-70% overnight travel The important thing for us is you ...

410 ICR United States USA

Sr. CRA

Saint Louis, MO

$110K - $138K/yr

Senior CRA - Ophthalmology - Midwest ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a ...

New

The Emmes Company, LLC

Sr. In-House CRA

Rockville, MD · On-site

... ophthalmology, rare diseases, and neuroscience. Through our two business units- Emmes, a full ... The Sr. In-House CRA may also be referred to as a Clinical Trial Associate on some contracts.

Emmes Group

Sr. In-House CRA

Rockville, MD · On-site

... ophthalmology, rare diseases, and neuroscience. Through our two business units- Emmes, a full ... The Sr. In-House CRA may also be referred to as a Clinical Trial Associate on some contracts.

Emmes

Sr. In-House CRA

Rockville, MD · On-site

Sr. In-House CRA Be Part of One Team, One Purpose. At Emmes Group, we're shaping the future of ... ophthalmology, rare diseases, and neuroscience. Through our two business units--Emmes, a full ...

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Ophthalmology Cra information

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$12

$22

$34

How much do ophthalmology cra jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for ophthalmology cra in the United States is $22.56, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $24.28 per hour, depending on experience, location, and employer.

What is an ophthalmology CRA?

An Ophthalmology CRA, or Clinical Research Associate in ophthalmology, is a professional who oversees and monitors clinical trials specifically related to eye diseases and treatments. They ensure that studies on new drugs, devices, or procedures for eye health comply with regulatory standards and study protocols. Responsibilities include monitoring patient safety, verifying data accuracy, and supporting investigators at clinical sites. Ophthalmology CRAs play a crucial role in advancing vision science and ensuring the integrity of ophthalmologic research.

What are the key skills and qualifications needed to thrive as an ophthalmology CRA?

To thrive as an Ophthalmology CRA, you need a background in life sciences or healthcare, knowledge of clinical trial protocols, and experience in ophthalmic research. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications like ACRP or SOCRA is typically required. Excellent organizational skills, attention to detail, and strong communication abilities help you manage study sites and ensure regulatory compliance. These skills and qualifications ensure the integrity of clinical trials and the safety of patients while advancing ophthalmic research.

What are some common challenges faced by ophthalmology CRAs when managing multiple clinical trial sites?

Ophthalmology CRAs often manage several clinical trial sites simultaneously, which can present challenges such as coordinating complex schedules, ensuring consistent protocol adherence across locations, and addressing site-specific regulatory requirements. Effective communication and organizational skills are essential to monitor data quality, resolve discrepancies, and support site staff. Additionally, since ophthalmic assessments may require specialized equipment or training, CRAs must stay up-to-date with advances in the field and ensure all sites are properly equipped and trained.

What is the difference between Ophthalmology Cra vs Clinical Research Associate?

AspectOphthalmology CraClinical Research Associate
CredentialsTypically requires life sciences degree, certification in clinical researchRequires life sciences degree, certification in clinical research
Work EnvironmentWorks in ophthalmology clinics, hospitals, research centersWorks in various clinical trial sites, hospitals, research organizations
Industry UsageSpecialized in ophthalmology studiesBroadly involved in multiple medical fields

Both roles require similar educational backgrounds and certifications, but Ophthalmology Cras focus specifically on ophthalmology clinical trials, working within eye care settings. Clinical Research Associates have a broader scope across various medical specialties, overseeing multiple types of clinical studies.

What are popular job titles related to Ophthalmology Cra jobs?

For Ophthalmology Cra jobs, the most frequently searched job titles are:

Infographic showing various Ophthalmology Cra job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $46,920 per year, or $22.6 per hour.

CRA II & Sr. CRA - Ophthalmology & General Medicine

Remote

Fortrea
Health Care and Social Assistance • 10K+ employees
Learn more about Fortreaexternal

$105/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 26 days ago

Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

30th of 75 rated research

Job description

We are currently seeking Experienced Ophthalmology (Sr CRAs & CRA 1/2) to lead and support our Full Service Outsourcing team. Open to major hub locations within the United States. 60-70% travel, 8-10 DOS per month.
WHAT YOU WILL DO
You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.
Responsibilities:
  • Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -
  • Responsible for all aspects of site management as prescribed in the project plans
  • General On-Site Monitoring
  • Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
  • Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
  • Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data
  • Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested
  • Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs
  • Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
  • Assist with training of new employees, eg. co-monitoring
  • Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned
  • Perform other duties as assigned by management

Requirements
  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
  • 1-3 years of Clinical Monitoring experience
  • Open to various hub locations

The important thing for us is you are comfortable working in an environment that is:
  • Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
  • Changing priorities constantly asking you to prioritize and adapt on the spot.
  • Teamwork and people skills are essential for the study to run smoothly.
  • Technology based. We collect our data directly into an electronic environment.

What do you get?
Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
  • Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
  • 401(K)
  • Paid time off (PTO) - Flex Plan
  • Employee recognition awards
  • Multiple ERG's (employee resource groups)
  • Target Pay Range (based on title): $105-140K

Work Environment:
  • Work is performed in an office environment with exposure to electrical office equipment.
  • Frequent travel to clients/ site locations with occasional travel both domestic and international.

Physical Requirements:
  • Ability to sit for extended periods and operate a vehicle safely.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
  • Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
  • Regular and consistent attendance.
  • Varied hours may be required.

#LI - Remote
Applications will be accepted on an ongoing basis.
Learn more about our EEO & Accommodations request here.

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