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Liquidia

Clinical-stage biopharma developing PRINT-based therapeutics

Senior Vice President, Head of Clinical Operations

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeUnited StatesNo salary listed

About the Job

Requirements

  • A bachelor's degree is required; a related field is preferred.
  • At least 15 years of progressive experience in clinical operations leadership within biotech or pharma is required.
  • Demonstrated success overseeing five or more clinical programs (Phase I–IV) simultaneously is required.
  • Experience leading multi-regional or global trials, including start-up through close-out, is required.
  • Deep understanding of pulmonary or respiratory therapeutic areas is required.
  • Ability to scale teams and establish efficient organizational structures is required.
  • Vendor management, budgeting, and operational governance experience is required.
  • The candidate should be based in or willing to travel frequently to the Raleigh–Durham area, or be an East Coast candidate.
  • Exceptional communication and change management skills are required.

Responsibilities

  • Define and implement the long-term vision, organizational design, and operating model for Clinical Operations.
  • Build, lead, and mentor a high-performing team capable of scaling with company growth.
  • Serve as a trusted member of the R&D leadership team, collaborating closely with Clinical Development, Regulatory, CMC, Clinical Quality, Commercial functions, and colleagues.
  • Serve as a strategic advisor to the executive leadership team.
  • Evaluate and implement emerging technologies and innovative trial methodologies to improve efficiency and patient experience.
  • Oversee planning, execution, and delivery of multiple concurrent clinical programs across development stages, including investigator-led and post-marketing studies.
  • Lead global study expansion, including country and region selection, feasibility, site activation, and oversight of regional contract research organizations and vendors; ensure compliance with local regulations, ethics committee requirements, import/export requirements for investigational product and samples, and data privacy laws.
  • Drive operational excellence to deliver programs on time, within budget, and in compliance with global Good Clinical Practice standards.
  • Optimize vendor relationships, including contract research organizations, central laboratories, and data management providers, for quality, accountability, and efficiency.
  • Ensure consistency across and within clinical programs.
  • Develop and manage departmental budgets, forecasts, and resource plans.
  • Implement metrics and dashboards to monitor performance, quality, and risk across studies.
  • Champion process improvement and innovation by introducing scalable tools and best practices.
  • Partner with Clinical Development, Regulatory Affairs, Safety and Pharmacovigilance, Clinical Quality, and Program Management to align operational strategy with corporate goals.
  • Contribute to program governance, study design input, and clinical strategy discussions.
  • Represent Clinical Operations in regulatory and partner interactions as needed.

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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