Clinical Research Coordinator (CRC)

Retina Center of Texas

Southlake, TXFull-timePosted Mar 12, 2026

40,800–58,250 a year

Behavioral Health Market Context

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Job Description

 obtained study images and save appropriate for study coordinator to upload to the reading centers
• Willing to assist in basic phlebotomy and lab processing. (Prior experience not required)
• Prescreen from clinic EMR to locate patients appropriate for enrolling trials
• Maintain lab kits and study supplies.
• Complete data entry and query resolution in a timely manner
• Communicate daily with patients as well as misc. Sponsor/CRO personnel in a professional manner.

Requirements and Qualifications
• CRC experience required.
• Ophthalmology clinical research experience preferred.
• Bachelors degree in scientific field or 2+ years of direct CRC experience.
• Team oriented mind-set.
• Ability to multitask, prioritize, and manage time efficiently
• Self-directed and able to work without supervision
• Proficient computer skills.
• Ability to work with the elderly, disabled and severely diabetic patients.
• Desire to continuously learn new things

Company DescriptionRetina Center of Texas’ premier team of board-certified, fellowship trained retina specialists are dedicated to treating retinal diseases with the most innovative treatments and surgeries available in the Dallas-Fort Worth Metroplex.

Qualifications

  • (Prior experience not required)
  • Prescreen from clinic EMR to locate patients appropriate for enrolling trials
  • CRC experience required
  • Bachelors degree in scientific field or 2+ years of direct CRC experience
  • Team oriented mind-set
  • Ability to multitask, prioritize, and manage time efficiently
  • Self-directed and able to work without supervision
  • Proficient computer skills
  • Ability to work with the elderly, disabled and severely diabetic patients
  • Desire to continuously learn new things

Benefits

    Responsibilities

    • Adhere to GCP, GDP, FDA and ICH guidelines
    • Effectively manage multiple clinic trials
    • Schedule patients for appointments and double-check that upcoming visits are within window
    • Maintain transportation needs and requests from patients, and schedule accordingly
    • Maintain and ensure the site specific binder is kept up to date
    • Compile obtained study images and save appropriate for study coordinator to upload to the reading centers
    • Willing to assist in basic phlebotomy and lab processing
    • Maintain lab kits and study supplies
    • Complete data entry and query resolution in a timely manner
    • Communicate daily with patients as well as misc
    • Sponsor/CRO personnel in a professional manner


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