Teams at Acadia Pharmaceuticals Inc.

Leads GCP quality assurance across Acadia’s clinical development portfolio. Responsibilities include planning and conducting audits of CROs, clinical sites, contract service providers, and vendors; managing audit reports, corrective actions, quality agreements, metrics, SOPs, and inspection readiness; supporting regulatory and mock inspections; advising cross-functional stakeholders on global GCP requirements; and improving quality systems and compliance processes.

Lead the enterprise AI platform and agent ecosystem, including multi-agent orchestration, reusable agent templates, self-service RAG, tool and skill registries, prompt management, evaluation frameworks, guardrails, and human-in-the-loop workflows. Partner with cybersecurity, architecture, governance, and business teams to deliver secure, scalable, compliant AI solutions. Drive adoption through low-code tooling, mentor engineers, and shape enterprise AI strategy across commercial, medical, R&D, and corporate functions.

Leads external R&D opportunity evaluations and scientific due diligence across neuroscience, psychiatry, and rare disease programs. Coordinates cross-functional input, develops diligence plans and integrated development scenarios, assesses scientific, clinical, regulatory, commercial, financial, and strategic factors, and translates findings into recommendations for senior leadership. Partners with Business Development on licensing, acquisitions, collaborations, and partnerships while supporting portfolio prioritization, governance materials, and consistent evaluation frameworks.