Study Coordinator
Job Summary
To support remote site activities for assigned projects, the part-time Study Coordinator will manage day-to-day communications, assist with recruitment and data entry, and ensure compliance with regulatory documentation while residing in or near High Point, NC.
Key responsibilities
- Serve as the main contact for site communications and activity coordination
- Support subject recruitment, re-consenting, and protocol activities as directed by the Principal Investigator
- Maintain compliance with IRB/FDA policies and assist with study closeout activities
Required qualifications
- Bachelor's degree or equivalent experience with a minimum of 2 years in a related field
- Current knowledge of ICH/GCP regulations and guidelines
- Experience with technology and web-based research platforms
- Ability to work independently and collaboratively with other team members
- Strong organizational skills and ability to multitask effectively
Complete Job Description
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