Clinical Research Coordinator II

4 weeks ago


Saint Petersburg FL, United States BayCare Health System Full time

Role Summary:

Clinical Research Coordinator II - Oncology is responsible for coordinating and implementing clinical research studies under the direction of the Principal Investigator in accordance with the standards of good clinical practice, federal and state regulations, and institutional review board (IRB) requirements.

Key Responsibilities:

  • Ensure adherence to the study protocol and schedule of events, patient visit scheduling for protocol-related procedures, screening, study recruitment, preparation of IRB reports, establishment and maintenance of regulatory documents, performing the process of informed consent and HIPAA authorization, clinical follow-up of study subjects, creation and completion of source worksheets, collecting source data for electronic data capture (EDC) systems or Case Report Form (CRF) completion, assessing patients for trial-related and non-trial-related symptoms, reporting of adverse events, and dispensing/accountability of investigational product.
  • Work independently and use sound judgment while performing job duties.
  • Perform other duties as assigned under the scope of related certification or licensure.

What We Offer:

  • Benefits (Medical, Dental, Vision)
  • Paid Time Off
  • Tuition Assistance
  • 401K Match and additional yearly contribution
  • Annual performance appraisals and team award bonus
  • Family resources and wellness opportunities
  • Community perks and discounts

Requirements:

  • Bachelor's Degree in a related field in lieu of experience and certifications
  • Associates Degree in a related field and CRC (Clinical Research) Radiology License, Cardiology License, RRT/Active NBRC (Respiratory), CRT/Active NBRC (Respiratory); with 2 years of Research Experience
  • High School Diploma/GED and CCRP (Clinical Research) or CCRC (Clinical Research) with 5 years research experience
  • Technical School Licensed Practical Nurse and LPM License with 5 years LPN experience and 1 year coordinator level role or 2 years LPN experience with 5 years research experience

Location: St. Petersburg, FL

Status: Full Time, Exempt: No

Shift Hours: 8:00AM - 4:30PM

Weekend Work: None

Equal Opportunity Employer Veterans/Disabled



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