Retina Clinical Research Assistant – Growth & Trials

Sacramento Native American Health Center, Inc; Modesto (CA); Vor Ort; USD 3.651.000 - 4.615.000; Vollzeit

Benefits dieser Stelle

PTO 13 days

7 Holidays

Scrub Allowance

401k Fidelity

Medical insurance 95% premium for the

Dental, vision, life, and accident

Zusammenfassung

Sacramento Native American Health Center, Inc seeks a full-time Research Assistant to support our clinical research team in a retina-focused clinical setting. You will work with physicians, patients, and sponsors to execute protocols per ICH-GCP guidelines and IRB-approved procedures, coordinating visits and data collection in a fast-paced environment.

Responsibilities include preparing visit documentation, monitoring subject flow, transcribing data, administering questionnaires, ECGs, and

Qualifikationen

• Education: High School diploma or the equivalent.
• Effective oral and written communication.

Aufgaben

• 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.
• 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 trial frame refraction and visual acuity testing.
• Perform other duties as assigned.

Kenntnisse

Effective oral and written comms

Ausbildung

High School diploma

Jobbeschreibung

Sacramento Native American Health Center, Inc seeks a full-time Research Assistant to support our clinical research team in a retina-focused clinical setting. You will work with physicians, patients, and sponsors to execute protocols per ICH-GCP guidelines and IRB-approved procedures, coordinating visits and data collection in a fast-paced environment.

Responsibilities include preparing visit documentation, monitoring subject flow, transcribing data, administering questionnaires, ECGs, and