Partner with us to lead GMP quality assurance for CMC programs, ensuring compliance and inspection readiness while mentoring a high-performing QA team in a dynamic clinical-stage environment.

Unlock potential by driving drug discovery through high-quality bioanalytical data. Collaborate with multidisciplinary teams to develop and execute LC-MS/MS assays for targeted protein degrader candidates, ensuring robust support for in vivo and in vitro studies.

Transform the CMC regulatory landscape for small molecules, guiding strategies from clinical development to market. Collaborate cross-functionally, author key submissions, and mentor junior staff while ensuring compliance with global standards.

Elevate pharmacovigilance operations by leading strategy, team development, and compliance. Oversee ICSR management, vendor relations, and inspection readiness while driving process improvements and ensuring safety data integrity across clinical portfolios.

Lead all phases of clinical trials with autonomy and support, managing teams and vendors to ensure successful execution, budgeting, and compliance while fostering strong collaborations with stakeholders throughout the process.