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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.

This role oversees quality assurance operations for drug manufacturing, focusing on stability programs, compliance, and regulatory interactions while managing cross-functional teams and external partners.

The Quality Operations Manager oversees quality assurance activities for drug production, ensuring compliance with regulatory standards and managing vendor performance.

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 Senior Statistical Data Scientist will develop, validate, and automate analytical pipelines, translating metadata into reproducible code, mentoring peers, and ensuring compliance for regulatory submissions.