Teams at Houston Retina Associates

Assists with clinical research visits under ICH-GCP and IRB-approved protocols. Responsibilities include scheduling subjects, preparing documentation, obtaining informed consent, collecting and entering study data, administering questionnaires, conducting ECGs and vision testing, processing biological samples, supporting patient care, resolving data queries, and assisting with adverse event reporting.

Provides comprehensive administrative support to a physician and Director of Research, managing complex calendars, meetings, travel, contracts, consulting invoices, memberships, CME records, financial disclosures, publications, and action-item tracking. The role requires discretion, strong organization, communication, editing, multitasking, and proficiency with Mac, iCal, Google Sheets, Adobe Acrobat, Microsoft Office, and practice management software.

Assists with clinical research patient visits under ICH-GCP and IRB-approved protocols. Coordinates subject appointments, prepares documentation, obtains consent, collects and records clinical data, transcribes information into electronic case report forms, administers questionnaires, performs ECGs and ophthalmic testing, processes biological samples, supports adverse event reporting, and helps resolve data queries.