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Key Responsibilities:
- Build and maintain integrated CMC timelines, ensuring alignment with clinical and regulatory milestones.
- Own CMC meeting cadence, track action items, and maintain a single source of truth for deliverables.
- Coordinate CDMO/CMO activities, budget tracking, and support regulatory submission timelines.
Experience and Skills:
- Bachelor's degree in a technical discipline; PMP or equivalent certification a plus.
- 5-8+ years of relevant experience in project or program management, with CMC or regulated industries preferred.
- Strong proficiency with planning tools like Smartsheet or Microsoft Project.
- Excellent organizational, facilitation, and communication skills; ability to influence without authority.
Work Environment:
- Remote position with periodic travel, supporting a lean, fast-paced biotech team.
- Collaborative and innovative culture as part of Roivant's family of companies.
- Opportunities to support broader program management as the company scales.
Pulmovant
Pulmovant is a clinical-stage biotechnology company focused on developing treatments for pulmonary diseases, with a lead candidate for pulmonary hypertension associated with interstitial lung disease. As part of the Roivant family, it fosters a collaborative and innovative culture, leveraging resources to advance its pipeline.