APAC/LATAM Regulatory Affairs Hematology Lead
Vor 4 Tagen
CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we're building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide.
Main Responsibilities and Accountabilities:
- The position holder is accountable for driving and implementing Innovative Regional Regulatory TA Strategies for the APAC/ LATAM TA.
- Driving and executing comprehensive, commercially and globally aligned regional regulatory activities across APAC/ LATAM Region for the TA.
- Accountable for CSL relationship with HA in the Region.
- Drive empowerment and capability-building initiatives for the TA team of RRL's, fostering informed decision-making and strong regional ownership.
- Establish and enhance effective communication channels and knowledge-sharing frameworks across local and global stakeholders.
- Represent Global Regulatory in regional or global health authority inspections and strategic meeting
Qualifications & Experience Requirements
- Advanced degree in Life Science or Business with a post graduate qualification (PhD, MD, MBA or other).
- 15+ years' experience in the pharmaceutical industry, at least 10 years' experience in Global Regulatory Affairs; biologics regulatory experience preferred.
- 10+ years' leadership experience, including managing global regulatory teams.
- Different qualifications or responsibilities may apply based on local legal and/or educational requirements.
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