Mô tả công việc:
About the role
We are looking for an experienced Regulatory Project Manager to independently manage global submissions, lead cross-functional teams, and support regional regulatory strategies. This role bridges global regulatory direction with local market execution and compliance.
Key responsibilities
- Independently manages submissions and supports major global regulatory filings.
- Leads cross-functional team meetings alongside regulatory leads.
- Develops, maintains, and tracks submission timelines; identifies critical paths and risks.
- Plans and facilitates kick-off and ongoing project meetings including agenda, coordination, and presentations.
- Documents meeting minutes, decisions, risks, and action items.
- Maintains project plans, dashboards, and collaborative workspaces.
- Supports regulatory activities related to contract manufacturing and product transitions, including partner coordination and compliance oversight.
- Leads scenario planning and risk mitigation activities.
- Tracks content plans with functional teams to ensure timely delivery.
- Manages rapid response processes for health authority queries.
- Supports advisory committee and health authority meeting preparations.
- Coordinates authoring, review, and approval of regulatory documents.
- Leads lessons-learned activities and maintains associated logs.
- Acts as subject matter expert for local and regional regulatory requirements.
- Supports localization of regulatory strategies and submissions per regional authority requirements.
- Ensures compliance with country-specific regulations, formats, and timelines.
- Provides translation support or review of submission documents in the local language, as needed.