Jobs · Healthcare · New York

RN, HCAT Administrator

University of Rochester · Rochester, New York Metropolitan Area · 1 mo ago
Healthcare$85k–$118k/yrFull-time

Responsibilities

  • Administrative, operational, and financial oversight of commercially available gene- and cell-based therapies.
  • Serve as the chair for both the HCAT Executive Steering and HCAT Operations Committees.
  • Coordinate cross-departmental assessment, implementation, and ongoing tracking of clinical, operational, and financial performance of HCAT-approved therapies.
  • Collaborate with finance, contracting, department administration, legal, pharmacy, nursing, and medical ethics to ensure successful and financially sustainable FDA-approved gene- and cell-based therapy programs.
  • Prepare quarterly reports summarizing all HCAT activity, including patient enrollment, clinical outcomes, costs, revenues, and new treatment entries approved.
  • Review all HCAT-related activities for new treatment approval, site qualifications, and patient qualifications.
  • Provide clinical and financial tracking for all HCAT-related activities.
  • Organize and oversee the timely site qualification and approval process with manufacturers or their designated third parties.
  • Engage UR Communications/PR to develop internal and external communications strategies for HCAT-approved products.
  • Develop a full business plan, including a 5-year proforma for treatments under review by the HCAT Subcommittee.
  • Update financial projections and overall business plans for HCAT-approved products as actual data becomes available.
  • Collaborate with payer contracting to ensure terms and conditions of all payer contracts are aligned with URMC standards for HCAT-approved products.
  • Maintain quarterly reporting on financial outcomes for all HCAT-approved products.
  • Ensure accurate, timely post-treatment tracking processes are in place to support financial performance at the individual patient and treatment levels.
  • Track patient activation process and serve as a liaison between clinicians, other departments, and patient/family, as needed.
  • Ensure effective tools are in place to track patients across the qualification, approval, contracting, and activation/treatment phases of care.
  • Ensure an accurate, timely post-treatment tracking process for clinical outcomes/metrics as specified in payer contracts, treatment protocols, or other industry standards.
  • Ensure all required training and education for HCAT-approved products are completed and documented before treatment is initiated.
  • Ensure all REMS regulatory requirements, as indicated, are being met and documented to ensure full compliance and audit readiness.
  • Facilitate and participate in cellular therapy quality committees and direct quality initiatives.
  • Ensure all requirements, standards, and regulations related to cellular therapies are met, in collaboration with the BMT Quality Manager.
  • Manage quality improvement opportunities, maintain data collection to meet program needs, and create standardization for program development.
  • Maintain interactions with clinical leads, research teams, and manufacturers, as well as FDA approval decisions and proceedings from symposia and conferences.
  • Serve as a liaison with manufacturers of cell- and gene-based therapies.
  • Foster effective communication with employees, peers, and leaders.
  • Manage projects, teams, and work groups related to HCAT therapies.
  • Establish a service culture to provide a first-rate experience for customers (patients, referring providers, faculty).
  • Ensure that staff across multiple departments receive job training and professional development in cell- and gene-based therapies.
  • Manage the change process.
  • Solve problems and make effective decisions using data/input from stakeholders.
  • Lead service improvement initiatives in the division.
  • Ensure that senior leadership goals and the hospital's strategic plan are communicated to staff and physicians.
  • Develop and maintain knowledge and competence related to cell- and gene-based therapies through continuing education, conferences, primary literature, liaison activities with peers, peer organizations, and manufacturers, and any other means necessary.

Qualifications

  • Master's degree in Nursing and 3 years of relevant experience in clinical practice required.
  • Equivalent combination of education and experience may be considered.
  • 2 years of experience in business planning, administration, or fiscal and resource management preferred.
  • Excellent project management skills, including collaborations across multiple departments preferred.
  • Strong independent leadership skills preferred.
  • RN licensure in NYS required upon hire.

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