Sr. Manager, Drug Safety & Pharmacovigilance Systems
About Acadia Pharmaceuticals
Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Position Summary The Senior Manager, Drug Safety & Pharmacovigilance will serve as the primary owner and subject matter expert for Acadia's Argus Safety Database, ensuring the system is secure, compliant, and optimized to support global safety operations. This critical role combines technical expertise, vendor management, and regulatory knowledge to maintain the integrity of safety data, enable efficient reporting, and support pharmacovigilance and regulatory submission activities. The PV Systems Senior Manager will lead all aspects of system oversight from daily operations and helpdesk support to vendor governance, upgrades, validation, and reporting. This individual will collaborate cross-functionally with IT, Quality, Clinical, and Regulatory teams to ensure seamless safety system performance, data integrity, and audit readiness. The role requires strong project management skills, deep understanding of PV workflows and regulations, and the ability to translate business needs into system solutions. As the Argus Safety Database owner, this position is central to ensuring that Acadia remains compliant with evolving global pharmacovigilance regulations while enabling proactive safety surveillance that ultimately protects patients. Primary Responsibilities- Execution of weekly, monthly and ad hoc reports from the PV database.
- Serve as the primary system owner for the Argus Safety Database, overseeing its configuration, maintenance, and performance.
- Manage the safety database hosting vendor, including service-level agreements (SLAs), issue resolution, change control, and compliance.
- Oversee the PV systems helpdesk and ensure timely resolution of user issues and support requests.
- Coordinate system upgrades, validation activities, and patch releases in collaboration with IT, Quality Assurance (QA), and the hosting vendor.
- Develop and maintain system documentation, including user guides, Standard Operating Procedures (SOP), and configuration specifications.
- Design, generate, and validate routine and ad hoc reports to support regulatory reporting, signal detection, and safety surveillance activities.
- Collaborate cross-functionally across departments and external stakeholders to ensure compliance with global regulatory requirements (e.g., FDA, EMA, MHRA, PMDA).
- Monitor and enforce user access controls, data security protocols, and audit readiness.
- Provide system training and onboarding support for Argus users.
- Represent PV Systems in audits, inspections, and cross-functional initiatives.
- Perform other duties as assigned.
- Experience managing external vendors and service providers.
- Strong knowledge of global pharmacovigilance regulatory requirements and ICH guidelines.
- Proficiency in safety database reporting tools (e.g., Argus Insight, SQL, OBIEE, Cognos).
- Understanding of system validation (CSV), change management, and audit readiness.
- Excellent analytical reasoning and problem-solving capabilities with the ability to solve problems.
- Excellent interpersonal and collaborative skills, with a professional demeanor, with the ability to interact with colleagues, cross-functional partners and vendors.
- Strong organizational and time management skills with the ability to multitask & prioritize own efforts.
- Must be able to travel domestically on occasion.
Physical Requirements
- Competitive base, bonus, new hire and ongoing equity packages
- Medical, dental, and vision insurance
- Employer-paid life, disability, business travel and EAP coverage
- 401(k) Plan with a fully vested company match 1:1 up to 5%
- Employee Stock Purchase Plan with a 2-year purchase price lock-in
- 15+ vacation days
- 13 -15 paid holidays, including office closure between December 24th and January 1st
- 10 days of paid sick time
- Paid parental leave benefit
- Tuition assistance
EEO Statement (US-based Employees): Studies have shown that women and people of color are less likely to apply for jobs unless they believe they meet every one of the qualifications in the exact way they are described in job postings. We are committed to building a diverse, equitable, inclusive, and innovative company, and we are looking for the BEST candidate for the job. That candidate may be one who comes from a less traditional background or may meet the qualifications in a different way. We strongly encourage you to apply, especially if the reason you are the best candidate isn't exactly what we describe here.
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