• Oversee the design and execution of a portfolio of research studies using a range of secondary data sources. • Lead and direct teams to conduct high-quality analyses, efficiently meeting task goals and project objectives. • Anticipate key risks and proactively develop and execute mitigating strategies. • Develop and prioritize recommendations based on expected impact, communicate risks and opportunities to ensure staff alignment, assume the role of final decision maker able to overturn decisions, and take accountability for outcomes. • Lead and strategize dissemination of research to a variety of stakeholders through peer-reviewed manuscripts, conferences, and other presentations. • Proactively manage client expectations and implement strategies to resolve issues on a client or project basis. • Anticipate potential opportunities by working collaboratively with clients and is perceived as a scientific partner, mentoring others to do the same. • Communicate roles, responsibilities, and expectations for staff; provide ongoing coaching to staff; handle challenging situations with tact and poise. • Support the growth of the business by contributing to and authoring research proposals and presentation content, participating in customer meetings, and targeting new opportunities with current customers for repeat business. • Manage communications to support department and business unit goals and objectives. • Partner with colleagues and business leaders on staffing decision recommendations (level to hire/when to hire) based on capacity models, utilization, and business pipeline. • Coach, mentor, and develop staff, including overseeing new employee onboarding and providing career development planning and opportunities. • Empower employees to take responsibility for their career development and goals.

Liquidia is deeply passionate and committed to the discovery, engineering, and development required to bring novel therapies to patients who need them most, and to the healthcare providers who care for them. Our current drive is toward improving the treatment of pulmonary hypertension (PH). We will continue to combine our proprietary, innovative PRINT® Technology with new and established medications, offering the potential for both better precision and improved clinical outcomes. Our team members include some of the industry’s top scientists, clinicians, business strategists, engineers, and pharmaceutical executives. We work together to help people lead longer, healthier, and happier lives. Job Summary We are seeking an experienced Associate Director, Clinical Supply, to join our growing Clinical Supply team. You will be responsible for developing clinical supply chain planning and forecasting to ensure continuous uninterrupted availability of supply throughout the development lifecycle including comprehensive global depot and site inventory management. You also will be responsible for supporting organizational infrastructure, including developing and implementing clinical supply chain procedures and other cross-functional and independent projects to support the developing pipeline. This individual will collaborate with internal and external partners to ensure uninterrupted material availability including providing CMO and IRT vendor oversight. Education and Experience - Bachelor’s degree or advanced degree in Life Sciences, Engineering, Supply Chain, or related field required - 8+ years of progressive experience with managing clinical supply activities including: bulk drug and device allocation planning, packaging and labeling forecasting and oversight, label creation/planning/design, global distribution and logistics, forecasting and demand planning and depot and site inventory management. - Proven experience supporting global clinical trials across all stages of development in multiple countries and regions (Phase I-III, IIR and post market) - Demonstrated hands-on experience with: - Global labeling and packaging strategies - IRT/RTSM system - Vendor and CMO management - Regulatory submissions related to clinical supply Knowledge, Skills and Abilities - Demonstrated aptitude for ‘hands-on’ operations with an exemplary history as a “self-starter” - Mechanical aptitude is a must, experience in the troubleshooting of production equipment preferred - Ability to read, interpret and create technical equipment documentation such as user manuals, electrical/pneumatic schematics, and fabrication drawings. - Experience with PLC and microcontroller programming and troubleshooting a plus - Must be detail oriented with excellent communication and documentation skills - Hands on experience with technical and/or experimental execution - Ability to interpret data and summarize results - Familiarity with statistical data analysis (DOE, process capability, hypothesis testing, ANOVA) a plus Global Clinical Supply Strategy & Execution - Develop and execute global clinical supply planning and forecasting for clinical trials across multiple countries and regions (e.g., North America, EU, APAC). - Lead clinical supply planning for assigned studies including forecasting, demand planning, labeling generation and approval, packaging and labeling operations oversight, material release and distribution, depot/site inventory management, IRT set-up and maintenance, expiry and dating extension management and cold chain/temperature excursion management. - Ensure supply strategies align with clinical timelines, protocol requirements, and regulatory constraints in each participating country. - Lead and perform demand and supply forecast modeling and scenario planning to enable comprehensive asset level and study level material and device planning. Operational Oversight - Manage end-to-end clinical supply activities, including: - IMP manufacturing coordination - Packaging, labeling, and blinding - Global distribution and depot management - Support returns, reconciliation, and destruction - Oversee Interactive Response Technology (IRT/RTSM) strategy and supply modeling. - Monitor depot and site inventory levels, manage resupply strategies, and mitigate supply risks to ensure continuous uninterrupted supply to patients. Vendor & Partner Management - Manage, and oversee CMOs, packaging vendors, depots, couriers, and IRT providers. - Establish and manage vendor scopes of work, budgets, timelines, and performance metrics. - Lead issue resolution and continuous improvement with external partners. Regulatory & Quality Compliance - Ensure clinical supply activities comply with global regulatory requirements (e.g., FDA, EMA, MHRA, PMDA) and GxP standards. - Support preparation and review of regulatory submissions and associated documents such as clinical label text, clinical trial protocol, pharmacy manual and IMPDs, INDs, CTAs. - Partner with Quality to support audits, inspections, deviations, CAPAs, and change controls. Cross-Functional Leadership - Serve as the clinical supply subject matter expert and primary point of contact on cross-functional clinical program teams. - Collaborate with Clinical Operations on study design considerations impacting supply forecasting and planning. - Work closely with CMC, Regulatory Affairs, Quality, and Manufacturing to align development and supply plans. - Provide comprehensive dynamic updates to internal and external partners on supply planning and forecasting, timelines, key risks and mitigations. Budget & Resource Management - Develop and manage clinical supply budgets. - Track and control costs while ensuring adequate supply and compliance. - Contribute to long-term clinical supply planning and organizational strategy. People Leadership (Associate Director level or as applicable) - Mentor and coach clinical supply team members. - Serve as a subject matter expert and develop continuous improvement plans, best practices, SOPs, and scalable processes to support pipeline growth. Liquidia offers a competitive compensation package as well as a comprehensive benefits package that includes Medical, Dental, Vision, STD, LTD, 401(k) Savings Retirement Plan, ESPP, and more! Liquidia is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Reasonable accommodation may be made to enable qualified individuals with disabilities to perform the essential functions of this position. Recruiting Agencies, Please Note:Liquidia will not accept unsolicited assistance from recruiting/search agencies for this employment opportunity. Please, no phone calls or emails. All resumes submitted by recruiting or search agencies to any employee at Liquidia via email, the Internet or in any form and/or method without a valid written search/recruitment agreement in place for this position will be deemed the sole property of Liquidia. No fee will be paid in the event the candidate is hired by Liquidia as a result of the referral or through other means.

• Develop, implement and continual evaluation of the Trade Distribution model to meet the needs of Protara customers and patients. • Own relationships with channel partners; leverage available data to identify trends and opportunities to improve distribution efficiencies, address risks and manage budget. • Oversee returns, adjusting transactions, new customer set-ups, credit limit requests, Trade notifications, and order reviews. • In partnership with IT, ensure quality of ex-factory sales data. • Oversee management of relationships and contracts with US Specialty Distributors. • Partner with Supply Chain to manage product dating and maintain appropriate inventory at 3PLs. • Liaise with Protara Legal team to ensure compliance to applicable laws and regulations. • Serve as a subject matter expert as a member of New Product Launch teams. • Partner with BD and Marketing to evaluate and recommend distribution strategies for new products. • Oversee Trade policies and procedures, such as orders, returns, replacements, credit/rebill requests, inventory, and chargeback processing. • Business travel by air, train, or car is required up to 50%.

• Lead strategy for NPR’s principal giving program • Build and maintain a robust pipeline of principal gift prospects • Conduct high-level prospect research and strategy development • Manage a portfolio of principal gift prospects and donors • Design and execute customized cultivation and solicitation strategies • Ensure exceptional stewardship of principal donors through high-touch engagement