Senior Manager, Program Management, PH-ILD

🕒 September 29

🇺🇸 United States – Remote

⏰ Full Time

🟠 Senior

📋 Program Manager

👻 Ghost score 25%

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Pulmovant

WebsiteLinkedInAll Job Openings

11 - 50 employees

🏥 Healthcare

💼 Consulting

🍽️ Food & Beverage

Healthcare • Consulting • Food & Beverage

Pulmovant is a company committed to transforming the lives of patients with pulmonary diseases by developing innovative therapies. Their lead product, mosliciguat, aims to provide a once-daily, inhaled treatment for pulmonary hypertension, distinguished by its novel sGC activation mechanism. With a singular focus on addressing the unique needs of patients suffering from pulmonary conditions, Pulmovant is engaged in extensive clinical trials to advance its pioneering treatment options.

📋 Description

• Lead and manage supporting PH-ILD studies, including Phase 1, biomarker, population PK, and nonclinical studies • Deliver studies on time, on budget, and to agreed quality standards through integrated project plans • Resolve issues and risks with team members and program stakeholders, escalating when necessary • Interact with cross-functional team representatives, Pulmovant program management members, and external partners • Establish and integrate program management tools, processes, initiatives, and documentation • Support cross-functional program planning, execution, monitoring, tracking, and reporting • Own day-to-day program management for supporting PH-ILD studies • Manage meeting and communication records, including agendas, minutes, charters, dashboards, and reports • Communicate effectively and manage time to meet stakeholder expectations

🎯 Requirements

• BS/BA degree in the health sciences required, with a demonstrated track record of success • 8 years experience in pharmaceutical drug development • 5 years experience directly managing and/or leading cross functional drug development teams • Drug development knowledge with frequent exposure to Research, Pre-Clinical, Clinical, Manufacturing and Operations, Commercial, Regulatory, Safety, and Payer functions • Understanding of Good Manufacturing Practices and Product Development Process requirements • Experience collaborating and influencing cross-functionally • Strong organizational and interpersonal skills • Strong planning and execution skills • Experience using MS Project, Smartsheet or equivalent required • Strong written and oral communication skills • Critical thinking and problem-solving skills • Demonstrated competencies in all aspects of project management • Proficiency with project management tools and analytics • Knowledge of applicable quality and regulatory standards requirements for the pharmaceutical industry

🏖️ Benefits

• Equal employment opportunities and prohibition of discrimination and harassment • Opportunity to make significant contributions to Pulmovant’s research and development programs