Jobs at Liquidia Corporation

Leads the strategic and operational execution of Liquidia’s global clinical pipeline across pulmonary and vascular diseases. Oversees multiple Phase I–IV programs, clinical operations strategy, team development, budgets, vendors, CROs, global trial execution, regulatory compliance, performance metrics, and process improvement. Partners with Clinical Development, Regulatory, Safety, Clinical Quality, Program Management, CMC, and Commercial teams while advising executive leadership and supporting innovative trial methodologies.

Provides executive scientific leadership for clinical pharmacokinetic and pharmacometric strategies across pharmaceutical development programs. Leads asset-level and study-level PK strategy, population PK and modeling analyses, inhaled drug development considerations, dose optimization, regulatory submissions, and CRO oversight. Partners cross-functionally with clinical, regulatory, biostatistics, CMC, and operations teams to translate quantitative findings into development decisions and regulatory recommendations.

Provides senior quality assurance leadership across pharmaceutical GxP operations. Leads complex investigations, complaints, change controls, risk assessments, quality records, corrective actions, and continuous improvement initiatives. Serves as a cross-functional quality subject matter expert, supports inspections and audits, interprets GMP requirements, improves quality systems, identifies systemic trends, and mentors colleagues without formal supervisory responsibility.

Supports pharmaceutical quality systems, including deviations, CAPAs, change controls, document management, GMP record issuance, and quality metrics. Reviews quality events, develops SOPs and work instructions, supports manufacturing and QC operations, provides quality systems training, monitors trends, identifies compliance risks, and contributes to inspection readiness and continuous improvement.

Leads Legal and Compliance department operations, including process improvement, legal technology administration, knowledge management, outside counsel and vendor management, budgeting, contract operations, reporting, compliance support, and insurance administration. Partners cross-functionally with Finance, HR, Commercial, Medical Affairs, Regulatory Affairs, and other teams to improve efficiency, scalability, risk management, and service delivery.

Manages and grows pharmaceutical sales within an assigned territory, representing pulmonary hypertension products to physicians and healthcare professionals. Responsibilities include achieving sales targets, tailoring customer interactions using disease and competitor knowledge, supporting patient access and reimbursement, developing healthcare partnerships, coordinating with cross-functional teams, and maintaining strict compliance with pharmaceutical laws and company policies. The role requires weekly travel throughout the territory and focuses on specialty or orphan disease commercialization.

Leads commercial new product planning, lifecycle strategy, brand planning, market research, competitive intelligence, and portfolio growth strategy for pharmaceutical pipeline assets. Shapes clinical development, evidence-generation, labeling, patient population, and access strategies while integrating market insights, financial modeling, and cross-functional input across Medical Affairs, Regulatory, Market Access, Finance, Analytics, and Business Development.

Executes Liquidia’s IT compliance program across SOX, GxP, and 21 CFR Part 11 requirements. Manages IT audits, control evidence, corrective actions, third-party risk assessments, infrastructure qualification, validated systems documentation, cybersecurity framework alignment, AI governance records, and external auditor coordination. Partners with Quality, Procurement, Legal, auditors, and IT stakeholders to maintain policies, assess compliance impacts, support validation activities, and mature the cybersecurity governance roadmap.