Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. This position serves a key leadership role in the organization as the portfolio program leader in support of the cross functional strategy for the programs (assets) in the Neuropsychiatry franchise. This role contributes

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. The Sr. Analyst is responsible for overseeing and driving key commercial, clinical and non commercial logistics and supporting related manufacturing operation activities (GMP and non GMP). He/she will coordinate and track

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary The Director of Regulatory Affairs (RA) Labeling will lead the development of a cross functional labeling strategy for products worldwide, including providing expert input on labeling requirements and str

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. The Sr. Medical Director will lead the development and execution of the medical strategy for Rett Syndrome. This will be accomplished by working in close collaboration with colleagues in Commercial, Regulatory, Market Acc

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. The Associate Director of Regulatory Affairs (RA) Labeling will assist in the development of a cross functional labeling strategy for products worldwide, including providing expert input on labeling requirements and strat

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. This position serves a key leadership role in the organization as the portfolio program leader in support of the cross functional strategy for the programs (assets) in the Rare Disease franchise. This role contributes to

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. This position will serve as a technology partner in the Research and Development (R&D) and Technology Development & Operations (TD&O) domains, providing technology leadership, operational support and project management fo

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Responsible for directing the regulatory aspects of internal and external communications including advertising and promotional activities as well as facilitation of labeling development, maintenance and distribution for a

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. The Director Regulatory Affairs position is responsible for developing and implementing global strategies to secure and maintain market approval for product(s) in the assigned development teams. Continually expands therap

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. The Director of Manufacturing is the Business lead, Technical Lead and primary contact responsible for managing Acadia's commercial Drug Product (DP) Contract Manufacturing Organizations (CMO's), and other third party sup

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Responsible for production planning, issuing forecasts and purchase orders to contract manufacturing sites, following up on orders to target on time delivery, support production requirements and inventory targets. Establi

Please note that this position is based in San Diego, CA AND/OR Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. The Director of Quality Audits & Compliance is responsible to independently lead, manage, and coordinate Quality GCP and GLP regulated activities and is responsible for performance of domestic and int

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. The Associate Director will support the strategic direction and oversee the tactical execution of operations for the Medical Affairs (MA), Rare Disease supporting the DAYBUE (trofinetide) launch and expansion efforts. Thi

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Responsible for supporting the overall strategy and approaches within Medical Safety and supporting the PV management on scientific topics, and interacting with Acadia executives/leaders with respect to issues related to

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Responsible for oversight of the outsourced analytical development activities associated with the development, validation, technology transfer, and line extension of drug product. Support pre formulation and drug product