As a RN, I have continued my education on the forefront of new technologies, and am currently enrolled in a MSN program and expect to graduate August 2013. My experience in my nursing career has placed me in a position of teaching and education to nurses, doctors and patients. At this point in my career, I would like to return to clinical aspect of patient care and am currently seeking a suitable position within my scope of practice where I can utilize my skills but still challenges me as a professional.
I have an extensive back ground in cardiology and electrophysiology which has given me experience in surgical/OR procedures, cardiac-cath lab, PACU, electrophysiology. Although my jobs have taken me outside the hospital, I still participate with patient care and education on weekly bases. During the years of research and development, I have worked closely in the electrophysiology labs with the doctors and staff during procedures. I have been training and have worked with ventilators, balloon pumps, hemodynamic monitory, and conscious sedation. I have also had expertise working in preclinical trial and clinical trials.
Currently seeking employment with mentorship that will foster growth as well as education to complement and expand my current knowledge base and experience. I am seeking collaboration with medical professionals to bring a more complete continuum of care to the patent population that is served by that physician and practice.
Cardiac Ablation/Electrophysiology Primary responsibility to support clinical trials of investigational electrophysiology technology. To include clinical education to physicians, nursing, and medical staff on equipment use and appropriate application. Training investigational site personal on the designed protocol for investigational devices. Responsible for guiding investigational sites through IRB process to establish investigational relationships for clinical studies. Responsible for education and training of the electrophysiology medical staff on the proper usage of medical equipment. Education of the doctors on the protocol and proper usage of the investigational equipment, and worked closely with site coordinators with education of study protocols and maintain study records. Conducted site initiation. Review and monitor regulatory documents at study sites. Followed up queries. Worked closely with coordinators and investigators to ensure an accurate and timely enrollment and maintain the timeline for completion of the study. Provided case support for all clinical procedures at assigned sites. Responsible for the accountability of all experimental disposables and equipment per FDA regulation and company standard of practice. Assist with management of site activities related to clinical studies. Serve as liaison between contracted research organizations, field sites, investigators, study coordinators and staff members. Provided technical assistance to study sites regarding the conduct of clinical research. Assist with clinical safety monitoring and site evaluation. Provide clear, concise, and accurate feedback of the clinical status of patients enrolled in clinical studies.
Participated in two IDE studies for ablation of Arial flutter and Arial fibrillation.