Sorry, this job is no longer accepting applications. See below for more jobs that match what you’re looking for!

Mds/Resident Assessment Coordinator

Expired Job

Avalon Health Care Group Honolulu , HI 96812

Posted 2 months ago

Avalon Health Care - Hale Nani is seeking an excellent part time MDS Nurse for a Resident Assessment Coordinator position!

The Resident Assessment Coordinator will be responsible for all of the facility Medicare and Managed Care residents as directed by the Resident Assessment Director. This will include the oversight of all service provided during inpatient stay from admission to discharge.

This position is also responsible for the accurate and timely completion of all OBRA required assessments. This role is viewed as a key financial and clinical member of the management team. This position will not be subject to nursing "call" schedules.

Candidates must have a current nursing license and familiarity with the RAI process and Case Management. The right individual for this position is good at building relationships and a good communicator.

Today's aging population means there's a growing demand for healthcare professionals in post-acute care, and a wave of career opportunities available at Avalon Health Care!

We are looking for individuals who embrace a reverence for life and a heart for healing. With enthusiasm and compassion, our Avalon family works with our patients and their families as well as with our communities to celebrate life every day!

If you seek to use your mind and your heart to improve lives on a daily basis, come join our team! We offer great challenges, a rewarding career and opportunities for advancement!

Job Requirements

  • Must have a current, active license to practice as a Licensed Practical/Vocational Nurse (LPN/LVN) or Registered Nurse (RN) in State of practice.

  • Must be well-versed in inter-personal communications

  • Must be familiar with the RAI process and Case Management

See if you are a match!

See how well your resume matches up to this job - upload your resume now.

Find your dream job anywhere
with the LiveCareer app.
Download the
LiveCareer app and find
your dream job anywhere
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Study Coordinator III Honolulu HI

Native Hawaiian Veterans

Posted 1 week ago

VIEW JOBS 12/7/2018 12:00:00 AM 2019-03-07T00:00 Native Hawaiian Veterans, LLC is a Native Hawaiian Owned, Service Disabled Veterans Owned Small Business (SDVOSB), SDB, MBE, UDBE, and EOE/W/M/Vet/Disabled Company that provides services, solutions, and products in the areas of Homeland Security, Emergency Management, Information Technology, Communication Equipment, Professional Staff Augmentation, Munitions and Explosives of Concern (MEC) Remediation, and Strategic Communications/Creative Services. Our mission is to be a trusted partner earning customer loyalty while fostering growth and profitability for our Ohana and enriching our community. We are seeking a Study Coordinator III to join our Ohana. This position will be located at Tripler Army Medical Center (TAMC) on Oahu. JOB DESCRIPTION * Supports the Department of Clinical Investigation (DCI), Tripler Army Medical Center (TAMC), providing non-personal services to specific clinical or translational studies, and shall provide input to the Principal Investigator (PI)/designated point of contact (POC). * Perform such duties to include, but not limited to: Identify potential clinical or translational studies. * Determine suitability of TAMC patient population based on inclusion / exclusion criteria and required timeline for study completion. * Match sponsored studies with appropriate Principal Investigator. * Provide input to the Principal Investigator with all Scientific Review and Institutional Review Board related requirements and any interface with clinical project collaborators or sponsors. * Assemble and make recommendations for clinical and translational study teams of study coordinators and other personnel needed to support the execution of the clinical study. * Collect, organize, maintain, and disseminate appropriate files of data as required and administer project, writing reports and preparing manuscripts. * Review patient records and identify potential eligible patients for inclusion/exclusion in the study. * Provide input to study subject enrollment, obtain specimens for laboratory analysis. Interface with other departments throughout TAMC (e.g. Pharmacy) in support of the clinical or translational study. * For possible future prospective trials, oversee consent process, monitor and assess patient response therapy. The Contractor shall ensure that all adverse events are noted and catalogued. * For translational laboratory or animal model studies, the Study Coordinator shall provide specimen collecting and processing. * Follow study subject course during study and interface with physicians, nurses and technicians to obtain up-to-date information about the study subject's status. * Shall assure that all case reports are completed accurately and in accordance with study sponsor requirements. * Retrieve appropriate data from patient's written and electronic medical records and extract patient information from computer data base, x-ray results, and laboratory/culture results, inputting this data into appropriate forms. * Assure that logs and collected data from patients enrolled in the study remain confidential. * Provide written reports of analyses which include evaluation of the statistical limitations of the available data and delineation of possible explanations of the findings. * Provide other written progress reports, deviation reports, continuing review reports, and updating of protocol approval documents as needed. * For data sets that are in electronic spreadsheet format, provide analyses within one (1) week. If data is provided as hardcopy and must be entered into a spreadsheet, an additional week is allowed to input the data. * Be able to read, write, and speak English well enough to effectively communicate with all parties and other health care providers. * In addition, if the position requires the use of computers, shall be computer literate. * Possess sufficient initiative, interpersonal relationship skills and social sensitivity such that he/she can relate constructively to a variety of patients from diverse backgrounds. * Remote Service if services are provided remotely, must adhere to all IT requirements for utilizing Government equipment and accessing Government systems. * Shall ensure that all supporting equipment is at it's own expense. i.e. interfaces, hardware, and software. EDUCATION/QUALIFICATION/EXPERIENCE * Education: Bachelors of Science in biomedical science field or nursing. * Experience: Minimum 10 years or successful execution of over 30 clinical trial studies or collaborative biomedical laboratory study experience. * Resume or curriculum vitae which reflects ability to conduct clinical and translational studies including the following: chart reviews, specimen processing, data management, interacting with physicians, scientists, nurses, and other laboratory personnel. * Ability to analyze data and summarize findings for incorporation into reports. * Must be able to prepare oral and written presentations (as reflected in resume by publications, posters or podium presentations at national conferences, delivery of lectures or scientific presentations, thesis) based on data analysis and study summary. * Demonstrated ability (i.e. former work history of managing multiple research studies or clinical trials) to manage multiple clinical and translational studies simultaneously, and develop policies and procedures for clinical study execution and oversight. * Experience with computers, to include ability to use Word and Excel, ability to retrieve information from computerized data system, development of tracking systems and maintenance of data and research records. * Research regulatory compliance experience with Institutional Review Board approvals, Human Research Protection Plans, Data and Safety Monitoring Boards, Quality Assurance of Research Execution. PREFERRED EXPERIENCE: * Biomedical post baccalaureate degree with clinical or translational study experience: M.D., Ph.D., or Masters Degree in biomedical sciences or health care profession. * Familiarity with statistical analysis and preparing manuscripts for publication. * Preferred experience in managing investigator-initiated, industry-sponsored, or military studies. * Preferred more than 5 years experience with coordination of collaborative partnerships, establishing networks of clinical and laboratory investigators, project management and laboratory analyses. To apply for this position, please complete our online Employment Application form by visiting http://nativehawaiianveterans.applicantpro.com/jobs/. Only applicants that apply via our Employment Application will be considered. Native Hawaiian Veterans, LLC is an EOE/W/M/Vet/Disabled. Native Hawaiian Veterans Honolulu HI

Mds/Resident Assessment Coordinator

Expired Job

Avalon Health Care Group