Transform regulatory policy strategy by leading a global team to enhance alignment, influence, and advocacy in support of R&D goals across diverse markets, driving impactful external engagements for the organization’s success.

Shape the future of cardiovascular development by leading global regulatory strategies. As a Senior Principal Scientist, you will drive approval processes for complex drug programs, serving as the strategic liaison with regulatory agencies worldwide.

Optimize global regulatory strategies for drug programs in cardiovascular metabolic areas. Lead cross-functional teams to secure approvals and navigate regulatory challenges effectively while fostering robust stakeholder engagement.

Champion global regulatory strategies for cardiovascular programs to achieve optimal labeling and expedite approvals. Leverage expertise in drug development while managing complex programs as a key regulatory contact across multiple markets.

Deliver high-quality statistical programming solutions for late-stage drug and vaccine development. Collaborate with global teams to create analysis datasets and reporting deliverables, ensuring compliance with industry standards and regulations.