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HTC Program Coordinator – Financial Reporting

Job in Memphis, Shelby County, Tennessee, 37544, USA
Listing for: Hemophilia Alliance Team
Full Time position
Listed on 2026-09-20
Job specializations:
  • Healthcare
  • Business
Salary/Wage Range or Industry Benchmark: 71000 - 127000 USD Yearly USD 71000.00 127000.00 YEAR
Job Description & How to Apply Below

The Program Coordinator – Financial Reporting is responsible for the coordination and delivery of program management activities supporting the Hemophilia Treatment Center (HTC). This role oversees data tracking, reporting, financial coordination, and cross-functional collaboration to ensure program goals and regulatory requirements are met. The coordinator serves as a key liaison across clinical, pharmacy, research (CRA), and administrative teams to support patient-centered initiatives and program sustainability.

Job Responsibilities:
  • Administer and coordinate one or more programs or projects within the HTC, ensuring alignment with organizational and departmental goals.
  • Define program and project requirements; identify interdependencies across clinical, pharmacy, finance, and external partners; and coordinate input from stakeholders.
  • Develop and maintain program communications, project plans, and operational processes.
  • Track key program metrics, including patient enrollment, financial performance, and program outcomes; analyze and interpret complex data to produce reports (e.g., biannual summaries, grant reports, operational dashboards).
  • Manage reporting related to program revenue, including tracking income generated through partnerships (e.g., specialty pharmacy programs) and documenting how funds are reinvested into patient care, education, and program initiatives.
  • Coordinate budget tracking, grant reporting, and financial reconciliation activities in collaboration with finance teams.
  • Facilitate collaboration between physicians, providers, pharmacy partners, and internal teams to support patient treatment programs and operational workflows.
  • Serve as a liaison between clinical teams and Clinical Research Associates (CRA) to ensure accurate and timely data submission and compliance with reporting requirements.
  • Support planning and execution of internal and external meetings, including annual meetings, regional administrative meetings, and committee meetings with pharmacy partners.
  • Contribute to the development and implementation of policies, procedures, and program initiatives.
  • Identify opportunities for process improvement and recommend solutions to enhance program efficiency, financial performance, and patient outcomes.
  • Engage with internal program management teams and external vendors/partners to support coordination efforts.
  • Maintain regular and predictable attendance; role is primarily onsite (Monday–Friday, 8:00 AM–5:00 PM).
  • Perform other duties as assigned to support departmental and institutional objectives.
Minimum Education and/or Training:
  • Bachelor’s degree required.
Minimum Experience:
  • Minimum requirement: 3+ years of experience in program management delivery.
  • Significant experience working with project planning tools (e.g., MS Project, Microsoft SharePoint, Service Now, Smartsheet, Clarity, Planview, MS Office).
Preferred Qualifications:
  • Familiarity with hemophilia care, rare disease programs, or patient populations served by a Hemophilia Treatment Center.
  • Experience managing or supporting healthcare-related programs involving clinical operations, specialty pharmacy partnerships, or patient services.
  • Knowledge of healthcare finance, budgeting processes, and revenue tracking, including experience managing program funds or grant-related budgets.
  • Experience with grant management, including preparation, submission, and reporting.
  • Demonstrated ability to analyze and report program performance data, including financial and operational metrics.
  • Experience working cross-functionally with clinical, research, and administrative teams in a healthcare or academic medical setting.
  • Strong understanding of regulatory or data submission processes (e.g., working with research/data management teams such as CRAs).
  • E…
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