Director, Clinical Operations

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 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 The Director, Clinical Operations will oversee the planning, execution, and delivery of clinical trials, initially focusing on our Yutrepia program, ensuring alignment with corporate goals and regulatory requirements. You will lead and closely work closely with internal and external stakeholders to bring transformative therapies to market with this new drug device combo treatment. The successful candidate will have extensive global clinical trial operational experience, an understanding of study set-up process and a deep understanding of patient pathways and trial recruitment. Proven expertise in setting up and executing a global, controlled trial in rare disease/device is critical. Engaging, building, and maintaining excellent working relationships with CROs and other vendors with critical oversight to help development and budgetary timelines is essential for this role. Education and Experience Bachelor’s degree required in the life or physical sciences. 10+ years of experience in clinical operations Proven track record of leading global clinical trials from start-up to completion Extensive clinical development and pharmaceutical experience with a base knowledge of the applicable regulations. Experience working on Phase 2-3 clinical development studies. Experience working in a fast-paced, innovative environment Highly desirable but not required: Experience supporting regulatory submissions, previous roles working as a study manager, study coordinator, research nurse, and working with rare diseases/devices. Knowledge and Skills Proficiency in Microsoft Office suite, basic computer and typing skills, and tools/systems for managing clinical trials. Strong written and verbal English communication and presentation skills. Excellent communication, collaboration and problem-solving skills Skilled at conflict resolution, collaborating with stakeholders with varying viewpoints, influencing with and without authority, and negotiation. Location/Travel This position is remote or office-based, depending on location. Travel may be required as needed to support the assigned clinical trial/s but would not be expected to exceed 15%. Leads on clinical and operational trial deliverables at trial sites according to timelines, budget, operational procedures, quality/compliance, and performance standards. Clinical Set-up and Execution Lead the strategy, planning, and execution of pivotal global clinical trials, ensuring quality, timeliness, and budget compliance Manage and mentor a growing clinical operations team, fostering a culture of excellence and accountability, including identification of ongoing resource needs over the lifecycle of a study Oversee selection and management of CROs, vendors, and clinical sites Develop and maintain clinical trial budgets, timelines and resource plans Collaborate closely with regulatory, medical, biometrics and CMC teams to ensure cross-functional alignment Ensure adherence to GCP, ICH guidelines, SOPs, and all applicable regulatory requirements Drive operational excellence through continuous process improvement and innovation Participate in clinical development strategy and contribute to regulatory submissions Clinical Trial Recruitment/Clinical Trial Health/Collaboration and Best practices Oversees and tracks patient recruitment for sites, proactively identifying ways to prevent delays. Supports the development of recruitment and retention plans in collaboration with regional CSM, oversight team and CRO. Reports local site situations and provides insights on recruitment challenges and solutions to regional personnel including regional clin ops, OSM and other members of the team. Oversees the activities of global and local CRO teams to ensure effective sponsor oversight of monitoring activities. Identifies trial issues and opportunities proactively, seeks solutions, and escalates them to the appropriate team members and management and leadership teams Collaborates with members of the Liquidia clinical and medical teams to share best practices and beneficial experiences. Supports CRAs and local CRO team members to aid trial delivery and compliance. Liquidia offers a competitive compensation package (base salary and commission) as well as a comprehensive benefits package that includes Medical, Dental, Vision, STD, LTD, 401(k) Savings Retirement Plan, ESPP, Unlimited Paid Time Off 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.