Registered Nurse- Clinical Research Coordinator

Employment Type: Full-Time, W-2 Employee
Location: Saint Petersburg, FL
Compensation: Competitive hourly rate; commensurate with experience
Schedule: Monday – Friday 

About Us:
Eirvera is a new and growing clinical research site dedicated to conducting high-quality clinical trials that advance medical knowledge and improve patient care. We are looking for a dedicated and skilled Nurse Practitioner (NP) to join our team as a Clinical Research Coordinator. This role offers a unique opportunity to contribute to cutting-edge research while providing patient care services.

Position Summary:
The Nurse will serve as a Clinical Research Coordinator, responsible for managing clinical trials in accordance with Good Clinical Practice (GCP) guidelines, sponsor protocols, and internal SOPs. In addition, the NP may perform protocol-required physical examinations and subcutaneous injections.

Responsibilities:

• Coordinate and manage day-to-day clinical trial activities at the research site including specimen collection and processing, ECG, informed consent, and conducting patient questionnaires
• Conduct patient screening, enrollment, and follow-up visits in compliance with study protocols
• Perform physical examinations and administer subcutaneous injections as required by study protocols
• Maintain accurate and up-to-date documentation in electronic case report forms (eCRFs) and study files
• Collaborate with physicians, study sponsors, monitors, and internal team members
• Ensure regulatory compliance and readiness for sponsor or regulatory audits
• Provide education and support to research participants
• Assist with study recruitment activities
• Maintain study supplies, study-related logs, including drug accountability and adverse event tracking
• Serve as liaison between the site, Sponsors, CROs , and other study representatives

Qualifications:

• Licensed Nurse in the State of Florida
• Minimum of 1 year of experience in clinical research preferred but not required
• Experience performing physical exams, blood draws, and subcutaneous injections required
• Knowledge of ICH-GCP, ICH guidelines, and FDA regulations a plus
• Strong organizational, communication, and interpersonal skills