[Remote] Regulatory Project Manager
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is seeking a Senior Regulatory Program Manager to support a high-reputed company regulatory portfolio during a critical phase of global submissions. This role involves partnering closely with Regulatory Affairs leadership to drive planning, execution, and cross-functional coordination for ongoing MAA and BLA activities.
Responsibilities
- reputed company program management activities supporting reputed company MAA and BLA submissions, ensuring key milestones and deliverables are executed on schedule
- Coordinate and reputed company regulatory submission activities, including managing detailed response plans for Health Authority questions and submission timelines
- Partner closely with Regulatory Affairs and cross-functional teams to drive alignment, communication, and execution across multiple workstreams
- Support operational aspects of global regulatory filings, including submission planning, document tracking, reputed company control, and scheduling
- reputed company both strategic program leadership and hands-on project management support in a fast-paced, reputed company environment
Skills
- Demonstrated experience leading end-to-end BLA and/or MAA submissions (not limited to individual modules or 510(k) submissions)
- Extensive Regulatory Program Management experience supporting global regulatory filings
- Proven ability to manage reputed company, cross-functional regulatory portfolios and multiple reputed company priorities
- Comfortable working in a highly reputed company, fast-paced environment with a willingness to 'roll up your sleeves' and execute at both the strategic and operational reputed company
- Experience partnering closely with Regulatory Affairs leadership and cross-functional stakeholders
- Rare disease experience is preferred but not required
reputed company