HCA Healthcare · 5 hours ago
Clinical Research Coordinator
Overland Park, KS
Full-time
Onsite
Entry Level
1+ years expHCA Healthcare is the nation's leading provider of healthcare services, and they are seeking a Clinical Research Coordinator to assist with all aspects of study implementation. The role involves coordinating research activities, managing clinical studies, and ensuring compliance with regulations, while also providing support to patients and staff throughout the research process.
BiotechnologyHealth CareHospitalMedicalPrimary and Urgent Care
Responsibilities
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 subjects 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 in EMR and appropriate hospital records
Assess and report adverse study events, including the IRB and any research sponsors Complete all paperwork affiliated with the study, including but not limited to the requirements of the facility, the IRB and the study Sponsor
Maintain copies of all research related correspondence
Conduct study activities helping to ensure all safety parameters
Ensure that all protocols activities are performed by approved research staff and ensure protocol compliance
Maintain professional relationships with sponsors, Clinical Research Organizations, research teams, pharmacies, laboratories, IRB’s, and hospitals for the coordination of research activities
Acquire continuing education pertinent to research and their licensed profession
Ensures compliance with and knowledge of the company’s Code of Conduct by all subordinates to ensure an ethical work environment
Practice and adhere to the “Code of Conduct” philosophy and “Mission and Value Statement.”
Qualification
Required
Minimum of one year clinical research experience
Coordinates and manages clinical studies according to OHRP and FDA regulations, as well as, ICH Good Clinical Practices and IRB requirements
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 subjects 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 in EMR and appropriate hospital records
Assess and report adverse study events, including the IRB and any research sponsors
Complete all paperwork affiliated with the study, including but not limited to the requirements of the facility, the IRB and the study Sponsor
Maintain copies of all research related correspondence
Ensure that all protocols activities are performed by approved research staff and ensure protocol compliance
Maintain professional relationships with sponsors, Clinical Research Organizations, research teams, pharmacies, laboratories, IRB's, and hospitals for the coordination of research activities
Acquire continuing education pertinent to research and their licensed profession
Ensures compliance with and knowledge of the company's Code of Conduct by all subordinates to ensure an ethical work environment
Practice and adhere to the 'Code of Conduct' philosophy and 'Mission and Value Statement'
Preferred
CCRC
RN License or Bachelor's degree in health related field
Benefits
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 AirMed 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.
Company
HCA Healthcare
HCA Healthcare provides medical education and healthcare services in locally managed facilities. It is a sub-organization of North Florida Endoscopy Center.
10001+ employees
Funding
Current Stage
Public CompanyTotal Funding
$8.51B2025-10-31Post Ipo Debt· $3.25B
2025-02-24Post Ipo Debt· $5.25B
2014-06-25Post Ipo Debt· $3.2M
Leadership Team
Nicholas Manning
Chief Executive Officer
Nick Lane
Regional Vice President Human Resources
Recent News
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