Ophthalmology Clinical Research Associate

Zp Group Llc

JOB DETAILS
SALARY
$90,000–$140,000 Per Year
SKILLS
Clinical Monitoring, Clinical Practices/Protocols, Clinical Research, Clinical Support, Clinical Trial, Data Quality, Detail Oriented, FDA Requirements, GCP (Good Clinical Practices), ICH Regulations, Maintain Compliance, Ophthalmology, Research Protocols, Risk Analysis, Site Initiation
POSTED
3 days ago

Piper Companies is seeking an Ophthalmology Clinical Research Associate to join a leading organization in the clinical research industry. The Ophthalmology Clinical Research Associate role is ideal for a detail-oriented professional with experience supporting ophthalmic clinical trials and ensuring compliance across study activities.

Responsibilities of the Ophthalmology Clinical Research Associate:

  • Support the planning, execution, and monitoring of ophthalmology clinical trials across multiple study sites.
  • Serve as a key point of contact for study teams, sites, and sponsors to ensure smooth communication.
  • Ensure trial activities adhere to ICH-GCP guidelines, FDA regulations, and study protocols.
  • Track study timelines, patient enrollment, and data quality while identifying and addressing risks.
  • Assist with site initiation, monitoring visits, and closeout activities.

Requirements of the Ophthalmology Clinical Research Associate:

  • 2+ years of clinical research experience with exposure to site or sponsor-side trial support.
  • Ability to travel to sites 8-10 days on site per month
  • 2+ years of onsite monitoring experience
  • Experience with ophthalmology or ophthalmic studies
  • Working knowledge of GCP, FDA regulations, and clinical trial processes.

Compensation for the Ophthalmology Clinical Research Associate:

  • $90,000 - $140,000 base salary , Depending on Experience and Level
  • Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.

Keywords:

ophthalmology, clinical research associate, CRA, clinical trials, GCP, FDA regulations, site monitoring, clinical operations, ophthalmic studies, CTMS, EDC, regulatory compliance, patient enrollment, study coordination

This job opens for applications on 07/17/2026. Applications for this job will be accepted for at least 30 days from the posting date.

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About the Company

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Zp Group Llc