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Clinical Trials Ophthalmology Jobs (NOW HIRING)

Glaukos

Sr. Clinical Trials Associate

Aliso Viejo, CA · On-site

$35.50 - $48.50/hr

The Sr. Clinical Trials Associate is responsible for the coordination of clinical research studies ... Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company ...

Glaukos

Sr. Clinical Trials Associate

Aliso Viejo, CA

$35.50 - $48.50/hr

Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company ... The Sr. Clinical Trials Associate is responsible for the coordination of clinical research studies ...

Glaukos

Sr. Clinical Trials Associate

Aliso Viejo, CA · On-site

$35.50 - $48.50/hr

Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company ... The Sr. Clinical Trials Associate is responsible for the coordination of clinical research studies ...

Glaukos

Clinical Trials Associate II

Aliso Viejo, CA

$35.50 - $48.50/hr

Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company ... Clinical Trials Coordination * Supports with the development of clinical trial protocols * Reviews ...

New

Glaukos

Clinical Trials Associate II

Aliso Viejo, CA · On-site

$35.50 - $48.50/hr

The Clinical Trials Associate is responsible for the coordination of clinical research studies in ... Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company ...

New

Glaukos

Clinical Trials Associate II

Aliso Viejo, CA

$35.50 - $48.50/hr

Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company ... Clinical Trials Coordination * Supports with the development of clinical trial protocols * Reviews ...

New

TMAC

$65K - $87K/yr

... trials • Provide clinical trial liaison support to site investigators involved in sponsored ... ophthalmology therapeutic area experience and/or Neurology Frequent travel is required.

CompHealth

Ophthalmologist

Minocqua, WI · On-site

Join a comprehensive ophthalmology practice in a picturesque northern Wisconsin town, surrounded by ... You will be part of a team with access to clinical trials, research, and academic affiliation.

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How much do clinical trials ophthalmology jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for clinical trials ophthalmology in the United States is $43.09, according to ZipRecruiter salary data. Most workers in this role earn between $36.54 and $43.03 per hour, depending on experience, location, and employer.

What challenges do professionals face in clinical trials ophthalmology, and how can they be addressed?

Professionals in clinical trials for ophthalmology often face challenges related to patient recruitment and retention, particularly due to the specific eligibility criteria and the need for regular follow-up visits. Ensuring high-quality, standardized imaging and data collection across multiple sites can also be complex. These challenges can be addressed by fostering strong communication within the research team, providing patient education to encourage engagement, and utilizing centralized reading centers for imaging analysis. Collaboration with investigators and adherence to best practices in protocol management are essential for overcoming these obstacles.

What are clinical trials in ophthalmology?

Clinical trials in ophthalmology are research studies that evaluate new treatments, medications, devices, or procedures for eye diseases and vision problems. These trials help determine the safety and effectiveness of new therapies for conditions such as glaucoma, diabetic retinopathy, macular degeneration, and other eye disorders. Participants in clinical trials may benefit from access to cutting-edge treatments while contributing to advances in eye care. The results of these studies guide clinical practice and help improve patient outcomes.

What skills and qualifications are needed to work in clinical trials ophthalmology?

To thrive in Clinical Trials Ophthalmology, you need a strong background in ophthalmic medicine, clinical research methodologies, and regulatory compliance, often supported by an MD or equivalent degree and experience in clinical trials. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and specialized ophthalmic diagnostic tools is essential. Attention to detail, strong organizational skills, and clear communication are crucial soft skills for ensuring accurate data collection and effective collaboration with multidisciplinary teams. These competencies are vital to maintain scientific integrity, adhere to regulatory standards, and advance ophthalmic research for better patient outcomes.

How to get into a clinical trials ophthalmology career?

To pursue a career in clinical trials ophthalmology, candidates typically need a medical degree (MD or DO) with specialized training in ophthalmology, along with experience in clinical research. Gaining certifications such as Certified Clinical Research Professional (CCRP) and developing skills in study design, data analysis, and regulatory compliance can enhance job prospects. Entry often involves working as a research coordinator or associate before advancing to more senior roles in clinical trial management.

Can you make a living doing clinical trials?

Clinical Trials Ophthalmology professionals can earn a stable income, especially with experience and specialized knowledge in ophthalmic research. Salaries vary based on location, employer, and level of expertise, and many work full-time for pharmaceutical companies, research institutions, or contract research organizations. Certifications and skills in clinical trial management and regulatory compliance can enhance earning potential.
More about Clinical Trials Ophthalmology jobs
What cities are hiring for Clinical Trials Ophthalmology jobs? Cities with the most Clinical Trials Ophthalmology job openings:
What states have the most Clinical Trials Ophthalmology jobs? States with the most job openings for Clinical Trials Ophthalmology jobs include:
What job categories do people searching Clinical Trials Ophthalmology jobs look for? The top searched job categories for Clinical Trials Ophthalmology jobs are:
Clinical Trials Ophthalmology jobs near you
Infographic showing various Clinical Trials Ophthalmology job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $89,619 per year, or $43.1 per hour.

Sr. Clinical Trials Associate

Glaukos

Aliso Viejo, CA • On-site

$35.50 - $48.50/hr

Full-time

Re-posted 7 days ago

Job description


The Sr. Clinical Trials Associate is responsible for the coordination of clinical research studies in compliance with U.S. and international regulations under the guidance of a Clinical Manager or Clinical Director.
Qualifications
What You'll Do:
The Sr. Clinical Trials Associate is responsible for the coordination of clinical research studies in compliance with U.S. and international regulations under the guidance of a Clinical Manager or Clinical Director.
  • Clinical Trials Coordination
    * Integral part of development of clinical trial protocols
    * Reviews clinical study data
    * Development of case report forms
    * CTA is responsible for effective communication with clinical trial sites
    * Uses gained experience to give high level analyses of study data
  • Reviews and Monitors Clinical Study Data
    * Reviews complex data as it comes in from sites
    * Documents errors and communicates to Manager and Director Clinical Operations
    * Communicates with sites to correct errors
    * Works with Manager with study management
  • Study Master File Maintenance
    * Sets up Study Master File and Study Master File Tracker at the beginning of each study
    * Receives, scans and files documents in Study Master File
    * Provides status of documents to Clinical Management
  • Collection of Site Start-Up Documents
    * Communicates directly with site staff to obtain site start-up documents
    * Prepares Regulatory Binders and provides to sites prior to Site Initiation Visit (SIV)
    * Obtains site documents from Regional Clinical Research Associates during trial
    * Receives, scans, and files site documents in Study Master File
    * Provides status of site documents in Study Master File to Regional Clinical Research Associates prior to Monitoring Visits
  • Establishes and Maintains Tracking of Critical Trial Information
    * Team and site contact information
    * Site status information
    * Enrollment trackers
    * Adverse event trackers
    * Site payment trackers and site payments
  • Team Support
    * Leads meetings internally and for investigative sites.
    * Perform site co-monitoring activities as needed.
    * Supports internal and external audits.
    * Schedules meetings, set up of AV, teleconference or video conference equipment
    * Preparation of relevant materials
    * Support IP shipment and shipment of other materials to sites

How You'll Get There:
  • Bachelor's Degree with background in science or equivalent work experience preferred
  • 5-8 years of work experiences as CTA in ophthalmic field required
  • Sr. CTA must demonstrate the following:
  • May have specific expertise i.e. systems subject matter expert, regulatory knowledge.
  • Ability to identify gaps and address them.
  • Understanding of the studies assigned; for instance can perform data cleaning.
  • Leading meetings internally and for investigative sites.
  • Able to perform site co-monitoring activities as needed.
  • Support internal and external audits required

#GKOSUS
About Us
Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible.
Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases.
Our mission at Glaukos is to truly transform vision by pioneering novel, dropless therapies that can meaningfully advance the standard of care and improve the lives of patients suffering from chronic, sight-threatening eye diseases.
Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients.
Our constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra "We'll Go First," which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do.
Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol "GKOS". Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente, California, and Burlington, Massachusetts.
Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
All offers of employment are contingent upon the successful completion of a background check, including successfully passing a drug screen, based on the position and local regulations.

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