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Role Overview

Conduct site visits (initiation, monitoring, close-out) and keep sites aligned with protocol and GCP.
Verify source data and help resolve queries quickly.
Provide training and serve as a go-to for site staff.
Enter and review clinical data in EDC.
Spot issues and inconsistencies early and follow through to resolution.
Help keep data flowing on time and accurate.
Support study start-up (reg docs, IRB/EC submissions, site set-up).
Maintain study files and trackers (eTMF, logs, spreadsheets).
Track enrollment, timelines, and key milestones.
Jump in wherever needed — from vendor coordination to preparing reports for leadership.

Requirements

2–4 years in clinical research (CRA, coordinator, or clinical ops).
Strong knowledge of GCP and basic regulatory requirements.
Comfortable with EDC, eTMF, and Excel/Google Sheets.
Sharp eye for detail and love of clean data.
A problem-solver who doesn’t wait to be told what to do.
Excited by startup life — resourceful, adaptable, and collaborative.

Tech Stack

Google Cloud Platform

Benefits

None specified

iSono Health

Open Positions (1)

Healthcare

Clinical Research Associate / Clinical Ops Coordinator