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Ophthalmic Research Assistant

North Carolina Retina Associates

  • Cary, North Carolina
  • 1 day ago
  • $23–$28

Highlights

The research assistant is primarily responsible for assisting in research patient visits according to International Council for Harmonisation Good Clinical Practice (ICH-GCP) guidelines and according to the Institutional Review Board (IRB)-approved study protocol and/or manual of procedures. Perform trial frame refraction and Early Treatment Diabetic Retinopathy Study (ETDRS) visual acuity testing (For Investigator Sponsored Trials (IST)s only, at selected sites).

Numbers & Facts

LocationCary, North Carolina
Salary$23–$28

Description

NC Retina Associates is looking for a Research Assistant to join our team! The research assistant is primarily responsible for assisting in research patient visits according to International Council for Harmonisation Good Clinical Practice (ICH-GCP) guidelines and according to the Institutional Review Board (IRB)-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.

Duties:
  • Coordinate and schedule subject visits within study/subject specific windows per protocol guidelines.
  • Prepare visit-specific documentation and charts for Clinical Research Coordinator.
  • Observe Coordinator in patient care and management.
  • Assist 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 (Phase 2 & 3; NO Gene Therapy).
  • Transcribe subject study information from source documents to the Electronic Case Report Forms.
  • Administer all mandatory questionnaires to study subjects.
  • Set up, prepare 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 Early Treatment Diabetic Retinopathy Study (ETDRS) visual acuity testing (For Investigator Sponsored Trials (IST)s only, at selected sites).
  • Inform subjects and obtain written re-consents in regard to Informed Consent Form (ICF)’s (selected studies)
  • Observe and assist scribe in ocular exams for doctors and confirm appropriate treatment per protocol.
  • Perform other duties as assigned.
  • Obtain any applicable additional/required sponsor training and/or certifications.

Minimum Qualifications:
  • High School diploma or the equivalent, with significant relevant experience.
  • College degree preferred.
  • Ophthalmic experience preferred.
  • Effective oral and written communication.
  • Delivers safe and appropriate care to patients in addition to the requirements outlined by study protocols.

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