Study Coordinator (Clinical Research)

Location: Remote, but must reside in or near High Point, North Carolina, United States

Employment type: Part time

Company

hirify.global provides consulting and operational solutions across regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology for biotech, medical device, and pharmaceutical organizations.

What you will do

• Coordinate day-to-day site communications, document submissions, and study activities.
• Support participant pre-screening, screening, and recruitment activities.
• Manage re-consenting, medical record collection, and protocol activities under Principal Investigator direction.
• Enter data, respond to system queries, and monitor clinical databases.
• Maintain site documentation in compliance with IRB and FDA policies.
• Support study closeout and other study-related activities.

Requirements

• Bachelor’s degree or equivalent experience, including at least two years of related education, knowledge, and skills.
• Ability to use web-based research platforms on a PC with Microsoft operating systems.
• Current knowledge of and ability to apply ICH/GCP requirements, applicable regulations, guidelines, SOPs, and global regulations.
• Strong verbal and written communication, critical thinking, organization, and multitasking skills.
• Ability to work independently and collaboratively, delegate tasks when needed, and follow directives.
• Requires a private remote workspace and residence in or near High Point, North Carolina.

Nice to have

• Clinical study team experience.

Culture & Benefits

• Remote working is supported, with hybrid collaboration encouraged for employees within a reasonable commute of an office.
• Inclusive workplace focused on diversity, equity, and inclusion.
• Environment encouraging innovation, collaboration, entrepreneurship, and individual authenticity.
• Applications are reviewed personally by the recruitment team rather than screened by AI tools.