Research Assistant
On-siteMorehead City, North Carolina, United States
Job Summary
Conduct study activities in compliance with GCP, SOPs, and protocols while monitoring participant safety and performing scheduled visits such as vitals and ECGs. Support recruitment efforts by screening participants, obtaining informed consent, and maintaining accurate documentation. Execute delegated clinical tasks including phlebotomy, sample collection, and point-of-care testing, while completing source documents, CRFs, and adverse event reports. Prepare for monitoring visits and audits, organize exam rooms and labs, and assist with scheduling and participant check-in/out. This hands-on role ensures studies run smoothly, safely, and in full compliance across 35 therapeutic areas within Centricity Research's centralized network.
Required Qualifications
- Have a degree in a health, science, or research-related field or equivalent hands-on experience in a healthcare or clinical setting
- Have strong attention to detail and can maintain accurate, compliant documentation
- Communicate clearly and professionally with participants, colleagues, and external partners
- Are tech-savvy and comfortable navigating Microsoft Office and clinical data systems
- Thrive in a team environment but can also work independently
- Bring a proactive, problem-solving mindset to every challenge
Desired Qualifications
- Are comfortable with clinical tools like blood pressure monitors, ECG machines, or point-of-care testing devices (or are eager to learn)
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