Lead the charge in AD&QC activities for late-stage oligonucleotide programs, ensuring regulatory submissions, compliance, and collaboration across teams to drive successful manufacturing and product quality standards in a dynamic environment.

Collaborate with cross-functional teams to lead regulatory writing efforts, ensuring high-quality documentation throughout the drug development lifecycle, from preclinical to registration stages, to support innovative medicine delivery.

Drive the future of clinical data management, ensuring excellence in data quality for multiple drug development programs. Lead and mentor teams effectively while collaborating with partners to meet critical project milestones and compliance standards.

Shape the future of employee engagement by enhancing onboarding and development initiatives, partnering with leaders, and driving HR strategies that foster a positive workplace culture and support organizational effectiveness.

Empower your career by supporting innovative statistical strategies and clinical trials, collaborating with stakeholders to enhance biostatistics functions, and driving impactful analyses that shape drug development and patient therapies.