Clinical Research Registered Nurse

HCA Healthcare

Chattanooga, TN

JOB DETAILS
SKILLS
Accounting, Advanced Cardiac Life Support (ACLS), Banking Services, Basic Life Support (BLS), Behavioral Health, Cardiology, Certified Clinical Research Coordinator (CCRC), Clinical Practices/Protocols, Clinical Research, Clinical Trial, Conduct Studies, Corrective Action, Customer Support/Service, Drug Dispensing, Electronic Medical Records, FDA Requirements, Flexible Spending Accounts, GCP (Good Clinical Practices), Healthcare, Hospital, ICH Regulations, IRB/IEC (Institutional Review Board/Independent Ethics Committee), Informed Consent, Laboratory, Laboratory Analysis, Medical Records, Medical Research, Nursing, Nursing Credentials, Organizational Skills, Orthopedics, Patient Care, Pharmacy, Philosophy, Phlebotomy, Prescription Drugs, Procedure Development, Protocol Analysis, Record Keeping, Registered Nurse (RN), Research Nursing, Research Protocols, Sample/Specimen Processing, Specimens/Samples, Stock Purchase Plans, Team Building, Telemedicine, Urgent Care
LOCATION
Chattanooga, TN
POSTED
Today

Do you want to join an organization that invests in you as a(an) Clinical Research Registered Nurse? At Chattanooga Orthopedics, you come first. HCA Healthcare has committed up to $300 million in programs to support our incredible team members over the course of three years.

Job Summary and Qualifications

GENERAL SUMMARY OF DUTIES: 

Responsible for assessing proposed study protocols and for the coordination and implementation of all nursing and administrative activities related to clinical trials. Performs within the parameters for which he or she is qualified by education, training, experience and licensure. 

SUPERVISOR: Practice Manager 

DUTIES INCLUDE BUT NOT LIMITED TO: 

 Coordinates all research study activities with the Principal Investigator and has 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. 

 Develops tactical study procedures 

 Develops any necessary study documents not provided by sponsor or IRB 

 Educates HCA staff regarding research and study protocols 

 Screens and recruits patients based on protocol criteria  Explains study protocols, procedures and treatments to patients and families 

 Conducts 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. 

 May function as Primary Coordinator for research studies 

 Responsible for all investigational drug accountability and dispensing 

 Coordinates with Pharmacist if on Delegation Log 

 Administers Investigational Drug as per protocol 

 Serve as a resource for department members for medical interpretations of research process and protocol specifics 

 Assess each proposed study protocol with critical analysis of potential implementation and patient care 

 Dedicate to creative/innovative growth of research in the division 

 Acquire continuing education pertinent to research and applicable licensed profession 

 Responsible for maintaining good clinical practice standards, addressing non-compliance issues, developing corrective action plans 

 Execute medical orders within parameters of education, training and licensure 

 Conduct study activities helping to ensure all safety parameters 

 Investigational device accounting and dispensing 

 Facilitate administrative review and approval of proposed studies 

 Provide/coordinate the highest level of contact, counseling and support services 

 Coordinate study activities and patient care with medical staff (cardiologist and PCP, etc.) 

 Implement and adhere to study protocol 

 Perform Phlebotomy and IV procedures 

 Prepare laboratory specimens for analysis, monitoring tests and procedures, shipping frozen specimens 

 Maintain patient records in EMR and appropriate hospital records 

 Assess and report adverse study events, included to 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 

 Maintain professional relationships with sponsors, Clinical Research Organizations, research teams, pharmacies, laboratories, IRB’s, and hospitals for the coordination of research activities 

 Review research and pertinent journals, abstracts and scientific literature 

 Practice and adhere to the “Code of Conduct” philosophy and “Mission and Value Statement”. 

EDUCATION: 

 Graduate of an accredited school of nursing or other health related field – required 

EXPERIENCE: 

 Minimum of two years’ experience in area of research specialty required. 

 Minimum of two years clinical research experience. 

CERTIFICATION/LICENSE: 

 Licensed RN 

 CCRC is preferred 

 BLS Certification; ACLS preferred 

 Actively maintained CCRC (Certified Clinical Research Coordinator) preferred

Benefits

Chattanooga Orthopedics, offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include:

  • Comprehensive benefits for medical, prescription drug, dental, vision, behavioral health and telemedicine services
  • Wellbeing support, including free counseling and referral services
  • Time away from work programs for paid time off, paid family leave, long- and short-term disability coverage and leaves of absence
  • Savings and retirement resources, including a 401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service), Employee Stock Purchase Plan, flexible spending accounts, preferred banking partnerships, retirement readiness tools, rollover support and financial wellbeing counseling
  • Education support through tuition assistance, student loan assistance, certification support, dependent scholarships and a partnership with Galen College of Nursing
  • Additional benefits for fertility and family building, adoption assistance, life insurance, supplemental health protection plans, auto and home insurance, legal counseling, identity theft protection and consumer discounts

Learn more about Employee Benefits

Note: Eligibility for benefits may vary by location.

Physician Services Group is skilled in physician employment, practice and urgent care operations. We are experts in hospitalist integration, and graduate medical education. We lead more than 1,300 physician practices and 170+ urgent care centers. We are HCA Healthcare’s graduate medical education leader. We provide direction for over 260 exceptional resident and fellowship programs. We focus on carrying out value-added solutions. These solutions help physicians deliver patient-centered healthcare. We support HCA Healthcare's commitment to the care and improvement of human life.

HCA Healthcare has been recognized as one of the World’s Most Ethical Companies® by the Ethisphere Institute more than ten times.   In recent years, HCA Healthcare spent an estimated $3.7 billion in cost for the delivery of charitable care, uninsured discounts, and other uncompensated expenses.


"Good people beget good people."- Dr. Thomas Frist, Sr.
HCA Healthcare Co-Founder

We are a family 270,000 dedicated professionals! Our Talent Acquisition team is reviewing applications for our Clinical Research Registered Nurse opening. Qualified candidates will be contacted for interviews. Submit your resume today to join our community of caring!

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

About the Company

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HCA Healthcare