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Manage analytical development projects, ensure compliance with GMP standards, oversee external partners, and support CMC stability programs in drug development.

Lead analytical development activities for drug products and substances, ensuring compliance with GMP standards and overseeing external providers. Collaborate with CMC teams to optimize processes and deliver product quality.

The Director, Quantitative Lead will guide statistical design and quantitative decision-making for clinical development at Praxis, leading teams and providing insights through advanced modeling methods.

Manage daily operations of Veeva systems, assist in user onboarding, execute Computer System Validation, and provide user support.

The Manager of Quality Management Systems oversees compliance with regulations, manages quality documentation, promotes continuous improvement, and ensures inspections readiness in partnership with cross-functional teams.

The Associate Director will lead BI&A research projects, translate data into strategic insights, and communicate findings to senior leadership within a fast-paced biopharmaceutical environment.

The Senior Manager oversees quality operations related to drug substance and product compliance, strategic quality decisions, and works with CMC teams for clinical and commercial quality activities.

The Senior Director of Market Access will develop and implement strategies for pricing, contracting, and payer engagement for product launches, leading a small team to ensure market access infrastructure is built effectively.

Lead the development and validation of analytical pipelines and statistical models, automate processes, mentor peers, and ensure compliance for clinical reporting.

The Associate Director will lead quality oversight for commercial and clinical supply chains, ensuring GMP compliance, and driving operational excellence across cross-functional partnerships.