Lead global safety strategy for complex oncology products. Mentor teams, manage risk analysis, and collaborate cross-functionally to enhance product safety across clinical and post-marketing phases. Drive key deliverables and compliance.

Oversee the development and execution of global regulatory strategies, ensuring high-quality submissions and compliance with health authority standards while collaborating with internal teams and external partners to achieve corporate goals.

Transform global regulatory strategies to meet asset goals and health authority requirements. Collaborate across teams to ensure high-quality submissions and mitigate risks while driving compliance in a dynamic regulatory landscape.

Shape strategic growth in oncology by leveraging relationships and market expertise. Drive commercial success across a complex territory, mentoring peers and fostering cross-functional collaboration to enhance product engagement and compliance.

Drive the end-to-end execution of CMC development and manufacturing activities, ensuring strategic alignment and timely milestones achievement while managing complex pharmaceutical and biotech programs across teams and partners.