Remote Clinical Study Coordinator - Research Operations

propharmagroup; United States; Hybrid; USD 60,000 - 90,000; Full time

Job summary

ProPharma seeks a Central Study Coordinator to support remote site activities for assigned projects. You will serve as the day-to-day contact for site communications, assist with pre-screening and recruitment, and ensure regulatory documentation aligns with IRB/FDA policies.

Responsibilities include data-entry, database queries, and coordinating with sites to maintain timelines. A Bachelor’s degree or equivalent experience is required, with strong communication and organizational skills.

Qualifications

• Bachelor’s degree or equivalent experience required.
• Understanding of ICH/GCP regulations and FDA policies.
• Experience coordinating clinical site activities preferred.

Responsibilities

• Serve as point of contact for day-to-day site communications and document submissions.
• Support pre-screening, screening and recruitment activities as assigned.
• Manage subject re-consenting, medical records acquisition and protocol activities.
• Perform data-entry and respond to system queries in clinical databases.
• Maintain timely site communications and regulatory documentation.
• Assist with study closeout and other site-related tasks.

Skills

Tech Proficiency

Strong Communication

Independent Work

Team Collaboration

ICH/GCP Knowledge

Education

Bachelor's degree or equivalent experience

Job description

ProPharma seeks a Central Study Coordinator to support remote site activities for assigned projects. You will serve as the day-to-day contact for site communications, assist with pre-screening and recruitment, and ensure regulatory documentation aligns with IRB/FDA policies.

Responsibilities include data-entry, database queries, and coordinating with sites to maintain timelines. A Bachelor’s degree or equivalent experience is required, with strong communication and organizational skills.