Registered Nurse - Clinical Research - Vaccine Study - Concord, NC
About The Position
Hawthorne Health is a leading community site network and home research visit solution provider, with 20+ sites and more than 2,000 research experienced healthcare professionals across the U.S. Hawthorne leverages convenient, trusted, healthcare locations, identified patient data, and intelligent technology to accelerate patient access, improve retention, and reduce study costs. By embedding high-quality research within local communities, Hawthorne makes clinical trials more accessible and convenient for patients. Our community-based model shortens timelines and helps bring better treatments to market, faster. WHAT YOU'LL BE DOING | THE ROLE Quality and safety outcomes assessments Administration of medication and/or investigational product Immediate postâadministration monitoring and adverse event identification/escalation Review of diagnostic and laboratory test results Participant education consults Accurate source documentation and delegated eCRF support Collection and processing of protocolârequired samples Performance of duties in compliance with protocol, GCP, and site SOPs Related professional clinical trial services as needed WHAT YOU BRING | THE PERSON Active, unrestricted RN license in the state of practice. 1â3+ years of recent, acute, or long-term care experience to operate independently. Experience administering vaccines. Certifications: BLS/CPR Strong clinical judgment, communication, and adaptability.
Requirements
- Active, unrestricted RN license in the state of practice.
- 1â3+ years of recent, acute, or long-term care experience to operate independently.
- Experience administering vaccines.
- Certifications: BLS/CPR
- Strong clinical judgment, communication, and adaptability.
Responsibilities
- Quality and safety outcomes assessments
- Administration of medication and/or investigational product
- Immediate postâadministration monitoring and adverse event identification/escalation
- Review of diagnostic and laboratory test results
- Participant education consults
- Accurate source documentation and delegated eCRF support
- Collection and processing of protocolârequired samples
- Performance of duties in compliance with protocol, GCP, and site SOPs
- Related professional clinical trial services as needed
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What This Job Offers
Education Level
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