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Director of Quality and Regulatory - Transplantation Services and VAD

122 302 - 155 933$
Формат работы
onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
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Описание вакансии

Текст:
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TL;DR
Director of Quality and Regulatory - Transplantation Services and VAD (Healthcare Quality and Regulatory): Overseeing quality improvement, regulatory compliance, and patient safety programs for transplant and VAD services with an accent on performance indicators, corrective action plans, and regulatory standards. Focus on analyzing clinical quality data, coordinating adverse event and mortality reviews, maintaining transplant policies, and preparing for CMS, UNOS, Joint Commission, and other regulatory surveys.

Location: Tufts Medical Center; normal office setting with frequent contact with patients, medical staff, and department personnel.

Salary: $122,301.82–$155,933.24 annually.

Company

Tufts Medical Center is an academic medical center, teaching hospital, and research institution providing specialty healthcare and transplant services across New England.

What you will do

  • Oversee clinical quality, patient safety, and performance improvement initiatives for the Transplant Program and VAD services.
  • Identify improvement opportunities, design performance indicators, analyze outcomes, and monitor quality metrics.
  • Coordinate corrective action plans resulting from surveys, root cause analyses, and other findings.
  • Plan and report adverse event reviews and coordinate transplant mortality and morbidity conferences.
  • Maintain current policies and guidelines for heart, kidney, liver, and VAD services.
  • Support quality management data systems, Epic dashboards, QAPI reporting, and SRTR data review.

Requirements

  • Master’s degree in Nursing, Healthcare Administration, Public Health, or a related health science field; or a bachelor’s degree in Nursing, Public Health, or a related field with eight years of related healthcare quality and regulatory experience.
  • Strong knowledge of healthcare quality improvement processes and regulatory compliance.
  • Experience with healthcare data collection, aggregation, analysis, chart reviews, and quality reporting.
  • Strong leadership, management, communication, analytical, and collaboration skills.
  • Ability to manage multiple projects, interpret clinical data, and present information to diverse audiences.
  • Proficiency with healthcare data systems and quality management software.

Nice to have

  • Quality and regulatory experience.

Culture & Benefits

  • Full-time employment in an academic medical center environment.
  • Opportunity to collaborate with physician leadership, surgery, data and informatics, and other departments.
  • Comprehensive Total Rewards package supporting health, financial security, and career growth.
  • Work includes participation in planned and unplanned regulatory surveys involving The Joint Commission, DPH, CMS, UNOS, and other agencies.

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