Clinical Research RN
Location: Overland Park, Kansas
Description: MMC â€" Midwest Heart & Vascular Specialists is at the momment seeking for Clinical Research RN right now, this job will be presented in Kansas. More complete informations about this job opportunity kindly see the descriptions. Job Number:
02134-18201 - ACQ)
Work Location
: United States-Kansas-Overland Park-MMC â€" Midwest Heart & Vascular Specialists
Schedule
: Full-time
Job Type
: Nursing - Professional
Description
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 all investigational 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:
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 Infor med 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
Ex ecute 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.)
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 activitie s 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
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 Ruleâ€, “GCPâ€, etc.)
Knowledge of medical coding and billing procedures in a physician practice setting.
Qualifications
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.
:
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If you were eligible to this job, please send us your resume, with salary requirements and a resume to MMC â€" Midwest Heart & Vascular Specialists.
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This job will be opened on: Fri, 23 Feb 2018 05:02:12 GMT