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Lead drafting, review, negotiation, and administration of commercial and G&A contracts. Partner with Commercial, Medical Affairs, Finance, and Compliance to improve CLM processes, templates, and workflows. Oversee contract execution, provide stakeholder guidance, manage intake and recordkeeping, and support CLM system design and training.

The Associate Director, Quality Assurance oversees GCP QA operations, conducts audits, supports clinical study activities, and ensures compliance with GCP regulations.

The Senior Scientist will develop and execute in vitro pharmacology assays, analyze data, mentor junior staff, and communicate findings to teams.

The Director, Global Product Leader oversees product development programs, manages cross-functional teams, and ensures strategic alignment for regulatory and commercial processes in the pharmaceutical industry.

The Scientist 1, In Vitro Pharmacology will develop cell lines, design pharmacology assays, analyze data, and mentor junior scientists.