Senior Manager, Program Management, PH-ILD

This is a fully remote position, open to applicants in United States.

📋 Description

• Lead and oversee the supporting PH-ILD studies, such as Phase 1, biomarker, population PK, and nonclinical studies.

• Ensure the timely, budget-compliant delivery of studies that meet established quality standards through comprehensive project plans.

• Address issues and risks alongside team members and program stakeholders, escalating matters when necessary.

• Collaborate with representatives from cross-functional teams, Pulmovant program management, and external partners.

• Develop and implement program management tools, processes, initiatives, and documentation.

• Assist in cross-functional program planning, execution, monitoring, tracking, and reporting.

• Take ownership of daily program management for the supporting PH-ILD studies.

• Maintain records of meetings and communications, including agendas, minutes, charters, dashboards, and reports.

• Effectively communicate and manage time to align with stakeholder expectations.

⛳️ Requirements

• A BS/BA degree in health sciences is required, with a proven history of success.

• 8 years of experience in pharmaceutical drug development.

• 5 years of experience in directly managing and/or leading cross-functional drug development teams.

• Knowledge of drug development with regular exposure to Research, Pre-Clinical, Clinical, Manufacturing and Operations, Commercial, Regulatory, Safety, and Payer functions.

• Familiarity with Good Manufacturing Practices and Product Development Process requirements.

• Experience in collaborating and influencing across functions.

• Exceptional organizational and interpersonal skills.

• Proficient in planning and execution.

• Experience with MS Project, Smartsheet, or similar tools is required.

• Strong written and verbal communication abilities.

• Critical thinking and problem-solving capabilities.

• Demonstrated proficiency in all areas of project management.

• Skilled in using project management tools and analytics.

• Knowledge of relevant quality and regulatory standards applicable to the pharmaceutical industry.

🏝️ Benefits

• Equal employment opportunities and a commitment to preventing discrimination and harassment.

• A chance to make meaningful contributions to Pulmovant’s research and development initiatives.