Austin-Clinical Research Assistant I

Austin Retina Associates • Austin, TX

2d

About The Position

Our goal is to advance retinal research, offer new treatment opportunities to our community, and provide the highest quality patient care. Austin Retina Associates is seeking curious and patient-focused individuals for a Clinical Research Assistant role. Our ideal candidate is passionate about patient care and is primarily responsible for assisting in research patient visits according to ICH-GCP guidelines and according to the IRB-approved study protocol and/or manual of procedures.

Requirements

• Master multiple computer systems including Google, Microsoft Office, Teams, data management
• Deliver safe and appropriate care to patients in addition to the requirements outlined in study protocol
• Ability to train and perform venipunctures and process samples
• Knowledge of and/or ability to learn ophthalmology and retina terminology
• High School Diploma or the equivalent, relevant experience, College degree preferred

Nice To Haves

• Strong interpersonal skills including effective listening, clear communication, effective customer problem resolution, warm encouraging demeanor
• Ability to develop and maintain effective relationships at work even in a high-paced, sometimes high-stress environment
• Demonstrate our core values: Serving with Compassion, Striving for Excellence, and Practicing Humility
• Excellent organizational and time management skills ensuring all tasks are completed in a timely manner satisfactory to the organization with ability to independently manage workflow
• Demonstrates high-level initiative and critical thinking skills
• Ophthalmic experience
• Bilingual in Spanish
• Experience with RealTime CTMS

Responsibilities

• Performs required trainings and obtains applicable certifications necessary to participate in specific study protocols including GCP, IATA, and other protocol-specific training
• Assist research coordinators to provide care for study patients, during visits, perform diagnostic testing, schedule appointments and educate patients regarding retinal condition, available treatment options and details of study protocol
• Perform data entry for multiple Electronic Data Capture (EDC) systems
• Train and certify in refraction and vision testing
• Inform subjects and obtain written re-consents in regard to ICFs
• Process and ship laboratory biological samples for analysis
• Perform intraocular pressure checks post injections
• Administer mandatory questionnaires to study patients
• Other duties assigned on an as needed basis delegated by Study protocol/Supervisor

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED
• Number of Employees: 51-100 employees