The Clinical Research Nurse Coordinator plays a key role in the smooth execution of multiple clinical trials through coordination and oversight ensuring compliance with established research protocols and standards. Additionally, this role will review study candidates’ medical records ensuring study eligibility and obtain proper consent from patients for clinical research studies. Responsibilities also include performing vital signs, venipuncture/phlebotomy, nasal swabs, and medication dispensing and tracking. Using good documentation practices, monitor and maintain case reports, forms, and charts that follow established SOP, GCP, and other applicable regulatory requirements.
WORK ENVIRONMENT
PHYSICAL DEMANDS
EDUCATION & EXPERIENCE:
REQUIRED
PREFERRED
TRAVEL
Less than 5% within the geographic region of the assigned work location
EEO STATEMENT
ERA Health Research (ERA) provides equal employment opportunities to all without regard to race, color, religion, sex (including sexual orientation or gender identity), national origin, age, disability, genetic information, or other protected status. Applicants and employees with disabilities may be entitled to reasonable accommodations under the terms of the Americans with Disabilities Act and certain state or local laws. A reasonable accommodation is an adjustment to our standard application and/or interview and/or employment process which will ensure an equal employment opportunity without imposing undue hardship on ERA. Please inform our team if you are requesting accommodation to complete any forms or otherwise participate in the application process or perform the essential functions of this role.
$27 - $60 per hour