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Clinical Research Coordinator

Georgia Retina
Posted 21 days ago, valid for 21 days
Location

Marietta, GA, US

Salary

Competitive

Contract type

Full Time

Paid Time Off
Disability Insurance
Employee Assistance
Flexible Spending Account
Employee Discounts

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Sonic Summary

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  • Georgia Retina is seeking a Clinical Research Assistant to support its high-volume Research Department focused on retinal care.
  • The position requires a minimum of 2 years of experience in healthcare, preferably in ophthalmology, though not necessarily in clinical research.
  • Responsibilities include recruiting and screening subjects, coordinating patient visits, and ensuring adherence to research protocols.
  • The role offers a competitive salary and a comprehensive benefits package, including medical, dental, vision, and a 401k with match.
  • Georgia Retina is an equal opportunity employer committed to diversity and inclusion in the workplace.

Company Overview

Georgia Retina, one of the largest retina-only medical practices in the Southeast, continues to provide patients with the most advanced medical treatments available for retinal diseases and disorders. With over 200 years of combined experience, Georgia Retina’s board-certified ophthalmologists offer world-class expertise and a personalized approach to patient care in 13 Metro Atlanta area locations.

Position Summary

We are now hiring for a Clinical Research Assistant that will support a high-volume Research Department within an ophthalmic practice that focuses on providing quality and compassionate care to each patient needing complete eye care services.

Responsibilities

A CRA is responsible for performing procedures and coordinating the execution of clinical trials in accordance with research protocols.

• Recruit and screen subjects to participate in trials• Coordinate patient visits and perform procedures related to research• Collect accurate data obtained from research visits• Monitor research participants to ensure adherence to study protocol• Adhere to Good Clinical Practice (GCP) guidelines including regulatory and ethical standards• Maintain relationships with site staff, study subjects, and sponsor delegates• Perform other related duties as assigned by the Clinical Research Coordinator• Maintain compliance with all research Standard Operating Procedures (SOPs)

Qualifications

Education and/or Work Experience Requirements:

• 2+ years in healthcare, preferably ophthalmology, but not necessarily in clinical research• Analytical mindset• Attention to detail• Exceptional interpersonal skills• Superior verbal and written communication skills• Understanding of laboratory procedures and equipment• Proficiency in MS Office – Word, Excel and Outlook• High school diploma or equivalent GED

Company Benefits

We offer a competitive benefits package to our employees:

  • Medical
  • Dental
  • Vision
  • 401k w/ Match
  • HSA/FSA
  • Telemedicine
  • Generous PTO Package

We also offer the following benefits for FREE:

  • Employee Discounts and Perks
  • Employee Assistance Program
  • Group Life/AD&D
  • Short Term Disability Insurance
  • Long Term Disability Insurance

EyeSouth Partners is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.




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