Project Coordinator I (non-IT)

Irvine, CA

The Fountain Group is a national staffing firm and we are currently seeking a ­­­­­­­­Part-Time Clinical Research Coordinator / Ophthalmic Study Support for a prominent client of ours.  This position is in Irvine, CA 92612. Details for the position are as follows:

Part-Time Clinical Research Coordinator / Ophthalmic Study Support

Irvine, CA (Onsite)
Part-Time | 16–32 hours/week
$27–28/hour

Our Client’s Eye Care Research Center is seeking a Part-Time Clinical Research Coordinator / Ophthalmic Study Support professional to assist with exploratory and clinical studies focused on patient experience and OTC eye care research.

This is a unique opportunity for someone with clinical research coordination and/or ophthalmic technician experience who enjoys working in a collaborative research environment with a mix of patient interaction, study operations, and clinical support responsibilities.

The team is open to candidates with a variety of backgrounds, including:

  • Clinical Research Coordinators
  • Ophthalmic Technicians (COA, COT, or COMT preferred)
  • Ophthalmology or Optometry clinic staff with research exposure
  • Study support professionals with patient scheduling, data entry, and operational experience

Schedule

  • Primarily onsite in Irvine, CA
  • Tuesday–Thursday availability required
  • Hours generally fall between 8:00 AM – 3:00 PM
  • Guaranteed minimum of 16–20 hours/week
  • Opportunity for additional hours up to 32–40/week depending on workload
  • Some remote administrative work may be available

Responsibilities

  • Support day-to-day execution of clinical research studies
  • Enter and maintain accurate study data and CRFs
  • Assist with protocol review and study preparation activities
  • Coordinate study files, inventory, supplies, and equipment
  • Support subject scheduling and study visit logistics
  • Assist with SOPs, work instructions, and operational processes
  • Perform study-related documentation and data cleaning activities
  • Conduct dry runs and ensure study readiness

Preferred Qualifications

  • Clinical research coordination experience
  • IRB submission and site-level research support experience
  • Ophthalmic technician certification preferred (COA, COT, or COMT)
  • Ophthalmology, optometry, or eye care experience strongly preferred
  • Strong organizational and operational skills
  • Comfortable working in a detail-oriented research environment
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