Lead global supply chain logistics for small-molecule clinical and future commercial programs. Oversee import/export trade compliance, customs brokers, freight forwarders, 3PLs, warehousing, distribution, KPI reporting, budgeting, continuous improvement, and team development to ensure timely delivery to patients and regulatory compliance.

The Associate Director of Scientific Communications will develop and review materials for medical and congress events, ensuring alignment with scientific standards. The role involves translating complex data into clear narratives, collaborating with various stakeholders, and maintaining compliance. Success depends on a strong scientific foundation and the ability to work in a fast-paced environment.

The Associate Director, Scientific Publications will develop and manage publication strategies, ensuring compliance and quality across various scientific communications and support clinical programs.

The Associate Director, Quality Assurance, GMP will ensure compliance with GMP regulations, manage quality systems, and collaborate with teams for drug development. Responsibilities include quality metrics evaluation, batch release operations, and preparing for regulatory inspections while maintaining effective relationships with stakeholders.

The Associate Director/Director of Quality Assurance for GCP will oversee quality activities related to clinical development programs, manage audits, ensure regulatory compliance, and lead quality initiatives across the company.

The Vice President of Regulatory Affairs will lead Commercial Regulatory Affairs and Regulatory Labeling, ensuring compliance with FDA requirements while guiding internal teams on promotional materials and product labeling.