- Suffolk, Virginia, United States
- On-site
- Full-time · Associate
Support the successful execution of clinical research studies from start to finish, involving participant recruitment, data collection, sample processing, and documentation.
Responsibilities
- Conduct study activities in compliance with GCP, SOPs, and protocols
- Monitor participant safety
- Perform scheduled visits and assessments (e.g., vitals, ECGs)
- Support recruitment efforts and screen participants
- Obtain informed consent and maintain accurate documentation
Requirements
- Degree in a health, science, or research-related field
- Equivalent hands-on experience in a healthcare or clinical setting
- Nice to have: Microsoft Office
- Nice to have: Clinical data systems navigation