Clinical Research Coordinator

Introduction

Do you have the career opportunities as a Clinical Research Coordinator you want with your current employer? We have an exciting opportunity for you to join Kansas City Card Arrhythmia Research which is part of the nation's leading provider of healthcare services, HCA Healthcare.

Kansas City Card Arrhythmia Research offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include:

• Comprehensive medical coverage that covers many common services at no cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free telemedicine services and free Air Med medical transportation.
• Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.
• Free counseling services and resources for emotional, physical and financial wellbeing
• 401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service)
• Employee Stock Purchase Plan with 10% off HCA Healthcare stock
• Family support through fertility and family building benefits with Progyny and adoption assistance.
• Referral services for child, elder and pet care, home and auto repair, event planning and more
• Consumer discounts through Abenity and Consumer Discounts
• Retirement readiness, rollover assistance services and preferred banking partnerships
• Education assistance (tuition, student loan, certification support, dependent scholarships)
• Colleague recognition program
• Time Away From Work Program (paid time off, paid family leave, long- and short-term disability coverage and leaves of absence)
• Employee Health Assistance Fund that offers free employee-only coverage to full-time and part-time colleagues based on income.

Learn More About Employee Benefits

Our teams are a committed, caring group of colleagues. Do you want to work as a Clinical Research Coordinator where your passion for creating positive patient interactions is valued? If you are dedicated to caring for the well-being of others, this could be your next opportunity. We want your knowledge and expertise!

The Clinical Research Coordinator (CRC) assists the principal investigator (PI) and sub investigators with all aspects of study implementation. Although the CRC is responsible for coordination of all activities related to clinical trial implementation, the CRC can only perform those procedures for which he/she is qualified by training and/or licensure.

• Coordinates all research study activities with the Principal Investigator and has no direct nursing care responsibilities.
• Coordinates and manages clinical studies according to OHRP and FDA regulations, as well as ICH Good Clinical Practices and IRB requirements.
• Assess each proposed study protocol
• Facilitate administrative review and approval of proposed studies
• Develop tactical study procedures
• Develop any necessary study documents not provided by sponsor or IRB
• Educate HCA staff regarding research and study protocols
• Screen and recruit patients based on protocol criteria
• Explain study protocols, procedures and treatments to patients and families
• Conduct the Informed Consent process in conjunction with study investigators
• Ensure that an original copy of any subject's Informed Consent Document is the in the research binders, as well as a copy on the subject's medical record.
• Provide/coordinate the highest level of contact, counseling and support services
• Coordinate study activities and patient care with medical staff
  
  Implement and adhere to study protocol
• Perform Phlebotomy and IV procedures
• Prepare laboratory specimens for analysis, monitoring tests and procedures, shipping frozen specimen Execute medical orders within parameters of education, training and licensure
• Conduct study activities helping to ensure all safety parameters
• Maintain patient records…