What are the responsibilities and job description for the Ophthalmic Clinical Research Assistant position at Scott and Christie Eye Associates?
Company Overview:At Scott & Christie Eyecare Associates, North Park Ophthalmology Associates, and Good Looks Eyewear, we are passionate about making a meaningful difference in our patients’ lives every day. Our team is dedicated to delivering exceptional eye care with compassion, respect, and personalized attention, while utilizing the latest advances in ocular diagnostics and treatment.
With convenient locations in Cranberry Township, McCandless, and Pittsburgh, PA, we proudly serve our communities with a full spectrum of services, including care for Cataracts, Glaucoma, Macular Degeneration, Diabetic Eye Disease, Dry Eye Disease, Routine Vision exams and contact lens fittings.
We are also actively involved in clinical trials, giving our team the opportunity to be part of innovative advancements and cutting-edge treatments in eye care.
Why Join Us?
When you join our team, you become part of a collaborative, supportive, and forward-thinking environment where your contributions truly matter. We are committed to professional growth, continuous learning, and providing the highest standard of patient care.
If you’re looking to build a rewarding career in healthcare and make a real impact, we’d love to hear from you. Come grow with us!
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.
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- 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:
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- 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 GEDCompany 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.
#IND
Work Location: In person
Salary : $39,742 - $61,487