Ophthalmology Clinical Research Associate

EyeSouth Partners; Gainesville (GA); On-site; USD 36,000 - 48,000; Full time

Benefits offered by this job

Medical

Dental

Vision

401k with Match

HSA/FSA

Telemedicine

Generous PTO

Employee Discounts

Employee Assistance Program

Group Life/AD&D

Short Term Disability Insurance

Long Term Disability Insurance

Job summary

North Georgia Eye Associates is seeking a Clinical Research Assistant to join our growing team in Georgia. The CRA will perform procedures and coordinate the execution of clinical trials in line with protocols, ensuring data quality and patient safety.

Responsibilities include recruiting and screening subjects, coordinating visits, collecting data, monitoring participants, and maintaining SOPs under GCP guidelines. Strong communication and attention to detail are essential.

Qualifications

• 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

Responsibilities

• 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)

Job description

North Georgia Eye Associates is seeking a Clinical Research Assistant to join our growing team in Georgia. The CRA will perform procedures and coordinate the execution of clinical trials in line with protocols, ensuring data quality and patient safety.

Responsibilities include recruiting and screening subjects, coordinating visits, collecting data, monitoring participants, and maintaining SOPs under GCP guidelines. Strong communication and attention to detail are essential.