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The Associate Scientist/Scientist in DMPK will develop bioanalytical methods and analyze samples for small molecule projects, collaborating with cross-functional teams.

The Director of Research Data Management will define and implement data management strategies, establish data standards, and lead data integration efforts that support drug discovery processes, partnering with various scientific teams.

The Senior Patent Agent will oversee the intellectual property portfolio, draft new applications, guide IP strategies, and support patent prosecution efforts.

The Associate Director of API leads API development for small molecules, managing drug substance activities in CDMOs, ensuring compliance with cGMP, and mentoring process chemists.

The Supply Chain Manager ensures timely supply and procurement of raw materials and drug substances, optimizing operations while meeting compliance and quality standards.

The role focuses on computational chemistry, employing molecular dynamics and cheminformatics for small-molecule drug discovery and optimization. Collaborates with multidisciplinary teams to influence therapeutic design.

Responsible for developing analytical methodologies and overseeing CMC projects for small molecule drug candidates to ensure regulatory compliance and quality results from CDMOs and CROs.

The Data Scientist will enhance the platforms, develop tools for clinical research, and ensure reliability of analytical solutions using software engineering best practices.

The Principal Data Scientist will lead the development of AI-powered data science tools, collaborating with cross-functional teams to enhance clinical research and optimize trials. Responsibilities include designing scalable solutions, ensuring software reliability, and communicating insights effectively.

The Associate Director/Director of Biostatistics provides statistical support for clinical drug trials, oversees CRO activities, and ensures regulatory compliance for data submissions.