Ophthalmology Photography Technician- Research
Sign up free to see how well your resume matches this role.
What you'll do
- 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)
What they're looking for
- 2-3 years in Clinical Research
- 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
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
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
EXPERIENCED 2-3 years in Clinical Research
• 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 (100% company paid)• EAP (100% company paid)• Group Life/AD&D (100% company paid)• STD (100% company paid)• LTD (100% company paid)• Generous PTO Package• 7.5 Paid Holidays• Flexible Scheduling• Employee Discounts and PerksWe are an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Company
Company facts come from this company's own listings. We only show what the postings themselves carry.