HCA, Hospital Corporation of America Clinical Research RN in Overland Park, Kansas

The HCA Physician Services Group (PSG) is the physician solution for the Hospital Corporation of America. PSG makes it easier for physicians to practice medicine by reducing the burdens of managing an independent practice and infusing the best clinical and operational standards in every office. With 13,000 employees that work in more than 790 practices across 21 states, PSG is leading the way by delivering high quality, cost effective health care in communities across the country.

We offer an excellent benefits package, competitive salary and growth opportunities. Join our team and share your skills and talents with the nation's largest private provider of healthcare services.

The Clinical Research RN coordinates all research study activities, while also being responsible for allinvestigational drug accountability and dispensing. They will also be required to maintain direct nursing care responsibilities.

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. RN license is required.

DUTIES INCLUDE BUT NOT LIMITED TO:

  1. Coordinatesall research study activities with the Principal Investigator and has direct nursing care responsibilities.

  2. Coordinates and manages clinical studies according to OHRP and FDA regulations, as well as, ICH Good Clinical Practices and IRB requirements.

  3. Developstactical study procedures

  4. Developsany necessary study documents not provided by sponsor or IRB

  5. EducatesHCA staff regarding research and study protocols

  6. Screensand recruitspatients based on protocol criteria

  7. Explainsstudy protocols, procedures and treatments to patients and families

  8. Conductsthe Informed Consent process in conjunction with study investigators

  9. 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.

    1. May function as Primary Coordinator for research studies

    2. Responsible for all investigational drugaccountability and dispensing

    3. Coordinates with Pharmacist if on Delegation Log

    4. Administers Investigational Drug as per protocol

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

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

    7. Dedicate to creative/innovative growth of research in the division

    8. Acquire continuing education pertinent to research and applicable licensed profession

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

    10. Execute medical orders within parameters of education, training and licensure

    11. Conduct study activities helping to ensure all safety parameters

    12. Investigational device accounting and dispensing

    13. Facilitate administrative review and approval of proposed studies

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

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

    16. Implement and adhere to study protocol

    17. Perform Phlebotomy and IV procedures

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

    19. Maintain patient records in EMR and appropriate hospital records

    20. Assess and report adverse study events, included to the IRB and any research sponsors

    21. Complete all paperwork affiliated with the study, including but not limited to the requirements of the facility, the IRB and the study Sponsor

    22. Maintain copies of all research related correspondence

    23. Conduct study activities helping to ensure all safety parameters

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

    25. Review research and pertinent journals, abstracts and scientific literature

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

KNOWLEDGE, SKILLS AND ABILITIES: This position requires the following minimum requirements:

  • Demonstrated leadership skills

  • Outstanding technical writing skills and understanding of medical terminology/research

  • Exceptional organizational, interpersonal, and presentation skills

  • Ability to communicate effectively with patients, clinical and administrative staff and the public

  • Ability to understand and follow complex, detailed technical instructions,

  • Ability to foster a cooperative work environment

  • Ability to maintain quality, safety, and/or infection control standards

  • Ability to understand and follow basic scientific research protocol and procedure

  • Ability to handle multiple priorities at once with minimal supervision.

  • Highly proficient with MS Office (Word, Excel, Access, and PowerPoint), email, internet

  • Advanced understanding of data management processes

  • Ability to analyze and interpret scientific data and skilled in the use of computerized systems and databases.

  • Knowledge of government regulations and compliance issues regarding clinical research and protection of human subjects (e.g. “Common Rule”, “GCP”, etc.)

  • Knowledge of medical coding and billing procedures in a physician practice setting.

    EDUCATION:

  • Graduate of an accredited school of nursing or other health related field.

CERTIFICATION/LICENSE :

  • Licensed RN

  • CCRC is preferred

  • BLS Certification; ACLS preferred

  • Actively maintained CCRC (Certified Clinical Research Coordinator) preferred

EXPERIENCE:

  • Minimum of two years experience in area of research specialty required.

  • Minimum of two years clinical research experience.

Job: *Nursing - Professional

Title: Clinical Research RN

Location: Kansas-Overland Park-MMC – Midwest Heart %26 Vascular Specialists

Requisition ID: 24232-65460