Research Assistant

The research assistant 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. Actives may be based on study and director's needs. This individual is responsible for providing accurate documentation, examinations, and professionalism. Responsibilities: • Coordinate and schedule subject visits within study/subject-specific windows per protocol guidelines. • Prepare visit-specific documentation and charts for the Clinical Research Coordinator • Observe the coordinator in patient care and management • Assist the Coordinator in monitoring subject flow and assist in subject care and management • Observe, assist, collect, and record all necessary data for follow-up (e.g., adverse events, concomitant • medications, etc.) study visits • Transcribe subject study information from source documents to the Electronic Case Report Forms • Administer all mandatory questionnaires to study subjects • Set up, prepare the subject, and conduct electrocardiograms (ECG) on subjects as required per study protocol • Promptly request all necessary medical records for Serious Adverse Event Reporting • Process and ship laboratory biological samples for analysis • Perform intraocular pressure checks after injections • Perform trial frame refraction and ETDRS visual acuity testing • Inform subjects and obtain written re-consents regarding informed consent forms (ICFs) • Perform other duties as assigned • Obtain any applicable additional/required sponsor training and/or certifications • Observe and assist the scribe in ocular exams for doctors and confirm appropriate treatment per protocol Qualifications: • Must be able to multitask • Critical time management skills • Certifications/Trainings • ICH GCP Training/Certificate • IATA Certification • Adhere to ongoing training and education • Demonstrate effectiveness showing courtesy, diligence, integrity, and teamwork. • Strong interpersonal skills (effective listening, clear communication, effective customer problem resolution, warm demeanor) • Providing training to both new and experienced colleagues is mandatory • Ability to lift more than 30lbs • Frequent use of a computer terminal, keyboard, and mouse • Manual dexterity to operate ophthalmic equipment • Other functions may be assigned, and management retains the right to add or change the duties at any time Compensation: $19.50 - $24.50 hourly

• Coordinate and schedule subject visits within study/subject-specific windows per protocol guidelines. • Prepare visit-specific documentation and charts for the Clinical Research Coordinator • Observe the coordinator in patient care and management • Assist the Coordinator in monitoring subject flow and assist in subject care and management • Observe, assist, collect, and record all necessary data for follow-up (e.g., adverse events, concomitant • medications, etc.) study visits • Transcribe subject study information from source documents to the Electronic Case Report Forms • Administer all mandatory questionnaires to study subjects • Set up, prepare the subject, and conduct electrocardiograms (ECG) on subjects as required per study protocol • Promptly request all necessary medical records for Serious Adverse Event Reporting • Process and ship laboratory biological samples for analysis • Perform intraocular pressure checks after injections • Perform trial frame refraction and ETDRS visual acuity testing • Inform subjects and obtain written re-consents regarding informed consent forms (ICFs) • Perform other duties as assigned • Obtain any applicable additional/required sponsor training and/or certifications • Observe and assist the scribe in ocular exams for doctors and confirm appropriate treatment per protocol