Remote Study Coordinator: Clinical Trials & Site Ops

PPG US ProPharma Group, LLC; Raleigh (NC); Hybrid; USD 52,000 - 76,000; Full time

Job summary

ProPharma is seeking a Central Study Coordinator to support remote site activities for assigned projects. The role requires coordinating day-to-day site communications, data entry, and regulatory documentation in accordance with IRB/FDA policies.

The candidate will assist with pre-screening, screening and recruitment, and may participate in study closeout while collaborating with Principal Investigators and cross-functional teams.

Qualifications

• Bachelor's degree or equivalent experience with at least 2 years related experience.
• Ability to work independently and in a team.
• Strong written and verbal communication.
• Knowledge of ICH/GCP regulations.
• Familiarity with SOPs and global regulations.

Responsibilities

• Serve as point of contact for day-to-day site communications and document submissions.
• Support pre-screening, screening and recruitment activities.
• Conduct subject re-consenting and obtain medical records.
• Perform data-entry and monitor clinical databases.
• Maintain timely site communications.
• Ensure documentation complies with IRB/FDA policies.
• Assist with study closeout and other study-related activities.

Skills

Remote work setup

Study Team experience

Critical thinking

Communication skills

Independent worker

Privacy conscious

ICH/GCP knowledge

SOPs compliance

Education

Bachelor's degree or equivalent

Job description

ProPharma is seeking a Central Study Coordinator to support remote site activities for assigned projects. The role requires coordinating day-to-day site communications, data entry, and regulatory documentation in accordance with IRB/FDA policies.

The candidate will assist with pre-screening, screening and recruitment, and may participate in study closeout while collaborating with Principal Investigators and cross-functional teams.