Remote Clinical Study Coordinator

ProPharma Group; High Point, Northern (NC, KY); Hybrid; USD 55,000 - 75,000; Full time

Job summary

ProPharma Group is seeking a Central Study Coordinator to support remote site activities for assigned projects and reside in or near High Point, NC. You will serve as the primary contact for site communications, assist with pre-screening, screening, recruitment, data entry, and regulatory documentation.

Responsibilities include coordinating protocol activities, acquiring medical records, and coordinating with the Principal Investigator.

Qualifications

• Bachelor's degree or equivalent experience.
• Minimum 2 years related combined education and experience.
• Knowledge of ICH/GCP and applicable regulations.
• Familiar with SOPs and global regulatory guidelines.

Responsibilities

• Coordinate day-to-day site communications and document submissions.
• Support pre-screening, screening and recruitment activities.
• Obtain medical records and conduct protocol activities as directed.
• Enter data and monitor clinical databases; respond to queries.
• Maintain timely site communication and regulatory documentation.
• Assist with study closeout and other duties as assigned.

Skills

Study Team experience

Critical thinking

Strong communication

Independent work

Privacy-aware working

ICH/GCP knowledge

SOPs/global regulations

Multitasking

Initiative

Education

Bachelor's degree or equivalent

Job description

ProPharma Group is seeking a Central Study Coordinator to support remote site activities for assigned projects and reside in or near High Point, NC. You will serve as the primary contact for site communications, assist with pre-screening, screening, recruitment, data entry, and regulatory documentation.

Responsibilities include coordinating protocol activities, acquiring medical records, and coordinating with the Principal Investigator.