Clin Ops Specialist

Overview

Supports clinical monitoring and operations activities for assigned studies, including site management, documentation, tracking, and coordination.

What you'll do

• Assist Clinical Monitoring staff with site management and site communications.
• Create and maintain Trial Master File and project files.
• Prepare and maintain site manuals, reference tools, and documents.
• Update clinical tracking information in databases.
• Track clinical and regulatory documents for sites and study teams.
• Manage the shared mailbox and route site correspondence.
• Coordinate site supplies, meetings, Case Report Forms, and queries.

What you'll need

• High School diploma or equivalent.
• Good communication skills.
• Good interpersonal skills.
• Ability to embrace new technologies.
• Ability to complete assigned clinical research training.

Details

• Remote in South Korea.
• Travel of up to 25% may be required.