Remote Study Coordinator - Clinical Trials & Site Ops

ProPharma; Raleigh (NC); Hybrid; USD 42,000 - 64,000; Full time

Job summary

ProPharma is seeking a Central Study Coordinator to support remote site activities and coordinate day-to-day site communications for assigned projects in or near High Point, NC. Responsibilities include screening support, data-entry, and adherence to IRB/FDA policies.

The role requires a Bachelor's degree (or equivalent) with 2+ years of related experience, knowledge of ICH/GCP guidelines, and the ability to work independently in a remote/hybrid setting.

Qualifications

• Bachelor's degree or equivalent experience (min 2 years related)
• Experience coordinating remote/site activities in clinical studies preferred
• Knowledge of ICH/GCP and applicable regulations

Responsibilities

• Coordinate day-to-day site communications, document submissions and activity coordination
• Support pre-screening, screening and recruitment activities
• Perform data-entry and monitor clinical databases as assigned
• Establish timely site communication and maintain documentation per IRB/FDA policies
• Assist with study closeout and other study-related activities as directed
• Work with site and CSCs to delegate tasks where needed

Skills

Strong communication

Critical thinking

Independent work

Team collaboration

Organization

Multitasking

ICH/GCP knowledge

Education

Bachelor's degree

Job description

ProPharma is seeking a Central Study Coordinator to support remote site activities and coordinate day-to-day site communications for assigned projects in or near High Point, NC. Responsibilities include screening support, data-entry, and adherence to IRB/FDA policies.

The role requires a Bachelor's degree (or equivalent) with 2+ years of related experience, knowledge of ICH/GCP guidelines, and the ability to work independently in a remote/hybrid setting.