RN Clinical Research Coordinator Eirvera LLC Saint Petersburg, FL Job Details Full-time $32 an hour 19 hours ago Qualifications Spanish Filing Care documentation Subcutaneous (SubQ) medication administration Physical assessments FDA regulations

Full Job Description 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 clinical coordinator 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 coordinator 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 Ability to work independently and manage multiple priorities Experience in using eSource Spanish speaker preferred

Job Type:

Full-time Pay:

$32.00 per hour

Physical Setting:

Clinic Experience:

ESource:

1 year (Preferred)

Language:

Spanish (Preferred)

Work Location:

In person