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Liquidia

Clinical-stage biopharma developing PRINT-based therapeutics

Director/Senior Director - Patient Support Programs

Biology & BiotechConfirmed live in the last 24 hours
Full-timeRemote in USANo salary listed

About the Job

Requirements

  • A bachelor's degree is required.
  • At least 8 years of experience in patient services, market access, reimbursement, or distribution within a pharmaceutical or biotechnology manufacturer is required.
  • At least 2 years of experience managing external patient support, HUB, or copay vendor relationships is required.
  • Demonstrated experience launching a patient services HUB and/or supporting a specialty product launch is required.
  • Strong familiarity with copay assistance, patient assistance programs, bridge and free drug programs, and financial support models is required.
  • Experience in access for a pharmacy benefit product is required.
  • Experience managing teams and in-line leadership roles is required.
  • Demonstrated understanding of healthcare compliance frameworks, including HIPAA, OIG guidance, and the federal Anti-Kickback Statute, is required.
  • Ability to travel up to 25% of the time for direct engagement with patient support vendors and partners is required.

Responsibilities

  • Provide the strategic framework and guidance for developing, deploying, and continuously improving patient support and affordability programs.
  • Design and maintain patient support programs covering reimbursement support, case management, adherence and persistency programs, nurse educators, copay assistance, patient assistance programs, bridge and quick-start free drug programs.
  • Develop annual patient support strategies and tactical plans with Market Access and Commercial leadership, aligning programs to brand strategy throughout each product lifecycle.
  • Monitor industry trends, including copay accumulators, maximizers, and Alternative Funding Programs, and incorporate their implications into program design, business rules, and gross-to-net planning.
  • Lead negotiation and execution of patient support program vendor agreements, including scope of work, business rules, service levels, and pricing.
  • Monitor key performance indicators and service level agreements—including time to first fill, benefits investigation accuracy, prior authorization turnaround time, adherence and persistency, and case closure rates—to ensure vendor partners meet contractual obligations.
  • Lead quarterly business reviews for patient support program vendors to assess performance and identify continuous improvement opportunities.
  • Manage day-to-day patient support program and vendor operations, including escalations, case-level issue resolution, and routine operational meetings addressing barriers to therapy initiation and continuity.
  • Develop, align, and maintain standard operating procedures and work instructions across patient support programs and specialty pharmacy partners to maintain operational consistency and quality.
  • Oversee patient assistance program eligibility criteria, income verification standards, and enrollment governance, including annual review and recertification.
  • Own patient support program reporting, including monthly and quarterly scorecards, program utilization, and enrollment funnel performance; translate insights into program enhancements and recommendations for commercial leadership.
  • Partner with Commercial Analytics and Finance on copay and free-goods forecasting, accrual support, and gross-to-net implications of affordability program design.
  • Partner with Marketing on developing, reviewing, and maintaining patient support program materials.
  • Collaborate with Market Access, Trade and Distribution, Field Reimbursement, Sales, Marketing, Medical Affairs, Quality, Pharmacovigilance, IT, Legal, and Compliance teams.
  • Ensure adverse event and product complaint intake, documentation, and reporting requirements are incorporated into program workflows and vendor training in line with pharmacovigilance obligations.
  • Address issues that may affect patient access, product initiation, or continuity of therapy with urgency.
  • Exercise sound judgment and oversight to ensure program integrity and compliance with company policies, HIPAA, OIG guidance, and the federal Anti-Kickback Statute.
  • Participate in company-sponsored meetings, trade shows, and industry conferences as requested by management.
  • Follow company compliance policies, procedures, and training requirements.
  • Perform other duties as assigned.

Desired Qualifications

  • Medical benefit or buy-and-bill experience is preferred but not required.
  • Direct experience building new patient assistance and patient support programs.
  • Experience in rare disease or orphan product commercialization.
  • Familiarity with pulmonary hypertension, including WHO Group 1 and WHO Group 3 disease states.
  • Understanding of pharmacovigilance integration and compliant patient education practices.
  • Experience with copay accumulator, maximizer, and Alternative Funding Program mitigation strategies.
  • Financial acumen in budgeting, forecasting, and profitability management.
  • Experience leveraging customer relationship management platforms and patient support performance analytics.
  • Experience working in a smaller or growth-stage biopharmaceutical environment.

About the Company

Liquidia

Clinical-stage biopharma developing PRINT-based therapeutics

Liquidia uses PRINT particle engineering to design drug particles that can improve safety, efficacy, and manufacturability. Its two main candidates are LIQ861 for pulmonary arterial hypertension and LIQ865 for local post-operative pain, developed through clinical testing toward commercialization. The technology controls particle size and properties to enhance delivery and performance while aiming to reduce production complexity and cost. By tailoring particle delivery for specific conditions, Liquidia pursues regulatory approvals to bring products to market and generates revenue from sales, supported by stock offerings for funding.

Company size
201-500
Company stage
IPO
Headquarters
Morrisville, NC
Founded
2004

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