Collaborate with a global regulatory team to develop and implement strategies for vaccine and infectious disease product submissions. Utilize excellent communication skills to engage with regulatory agencies and support cross-functional initiatives.

Lead the charge in shaping global Regulatory CMC strategies for synthetic moieties in ADCs, ensuring compliance and successful delivery of regulatory milestones across product development and lifecycle management.

Drive innovative bioanalytical strategies while leading a team of experts in drug discovery. Contribute to biologics projects in immunology and oncology, optimizing approaches and collaborating across multi-disciplinary teams.

Engineer impactful QP2 oncology strategies, mentor scientists, and guide drug development decisions. Shape clinical programs through quantitative science, regulatory interactions, and interdisciplinary team leadership to advance patient outcomes.

Champion compliance and performance in clinical research sites, ensuring protocol adherence and quality standards while fostering relationships with stakeholders and developing new clinical study sites across territories.