Research Assistant - Unmasked

Retina Consultants of Houston•Katy, TX

18d•Onsite

About The Position

Retina Consultants of Texas is seeking an Unmasked Research Assistant for its Katy location. The role assists with research patient visits in accordance with ICH-GCP guidelines and IRB-approved study protocols or manuals of procedures. Day-to-day duties may vary based on the employee’s experience and knowledge and the organization’s needs. The Research Assistant supports patients and providers during the Research Department’s operating hours of 6:30 a.m. to 5 p.m., Monday through Friday. Weekly schedules depend on provider clinic, patient, and surgery schedules. The position supports Phase 2 and 3 study visits (excluding gene therapy), including preparing subjects for treatment, assisting with treatment and follow-up, collecting and documenting study data, and helping maintain equipment and treatment areas. The role requires knowledge of eye anatomy, ocular conditions and medications, strong organizational and communication skills, attention to detail, and the ability to manage workflow and priorities. The starting pay rate is $19.00 per hour, and the role is eligible for overtime. Full-time eligible employees receive the described benefits after a 60-day introductory period, with certain benefits available from the hire date. Retina Consultants of Texas describes its culture as emphasizing Hard Work, Authentic Care, and Innovation.

Requirements

High school diploma or equivalent required.
Three years of ophthalmology experience.
Working knowledge of eye anatomy, disease, symptoms, and ocular medications.
Excellent organizational skills and ability to independently manage workflow.
Meticulous attention to detail.
Initiative and ability to prioritize quickly.
High-level critical-thinking skills.
Ability to work positively and professionally with supervisory staff, physicians, peers, external customers, and patients.
Excellent personal and written communication skills.
Organizational and time-management skills, including multitasking.
Ability to stand for long periods.
Ability to write.
Ability to hold arms at shoulder height.
Ability to communicate by telephone.
Manual dexterity to work with ophthalmic equipment.

Nice To Haves

College degree preferred.
Level II or III Unmasked Research Assistant preferred for reporting treatment-related adverse events.

Responsibilities

Conduct safe and appropriate aseptic and sterile-field techniques.
Assist the Coordinator in monitoring subject flow and providing subject care and management.
Observe, assist, collect, and record necessary follow-up study-visit data, including adverse events and concomitant medications.
Ensure treatment rooms are stocked with ancillary supplies before each day.
Explain treatment processes and procedures to study subjects.
Set up and prepare subjects and assist with treatment administration as required by the study protocol and pharmacy or procedure manual.
Promptly report treatment-related adverse events, including medication errors, to an appropriate unmasked Research Assistant.
Assist with collection of aqueous humor samples for analysis.
Perform intraocular pressure checks after injections.
Perform post-treatment procedures, including finger count, hand motion, and light perception checks.
Monitor on-site temperatures for equipment and document daily logs, if applicable.
Calibrate tonopens daily.
Obtain applicable additional or required sponsor training and certifications.
Ensure all instruments used by the unmasked team are accounted for and properly sterilized.
Perform other duties as assigned.