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The Director of Pharmacometrics will advance drug development, lead analyses, and contribute to regulatory submissions, ensuring quality and timely deliverables.

The Legal Operations Manager supports contracting activities and patent administration, manages contract workflows, drafts contracts, and coordinates with legal teams.

The Associate Director of GMP Quality Assurance is responsible for ensuring compliance in drug substance manufacturing, mentoring junior staff, and collaborating with various departments to ensure quality standards are met.

Lead the design and implementation of QMS and CSA frameworks, ensuring compliance with GxP regulations and overseeing quality management processes and software assurance.

The Senior QC Specialist conducts comprehensive QC reviews of analytical data to ensure compliance and integrity for drug substance and product programs, collaborating with Quality Assurance and Manufacturing teams.

The Associate Director, GxP Training leads the development and improvement of GxP training programs, ensuring compliance with regulations and integrating quality performance data. They partner cross-functionally to align training with quality objectives while driving continuous improvement initiatives and overseeing training operations and documentation.

This role involves providing strategic QA oversight of drug substance manufacturing, ensuring GMP compliance, and aligning quality strategies across teams. Responsibilities include document review, deviation management, and vendor interactions.

Lead global GCP quality strategy and oversight for sponsor and outsourced clinical trials. Develop audit strategy, provide GCP guidance, make final quality decisions, manage vendor/CRO risks, ensure inspection readiness, and drive continuous improvement of GCP QMS and training to protect patient safety and data integrity.

Join a team focusing on membrane protein expression and purification to support drug discovery. Responsibilities include construct design, GPCR purification for cryo-EM, and data analysis.

Lead CADD/SBDD strategy for discovery programs, translate structural insights into testable design hypotheses, apply CADD methods (docking, MD, FEP+), partner with structural biology, medicinal chemistry, DMPK and platform teams, and mentor scientists to accelerate S-DMTA cycles.