Senior Associate R&D Quality and Risk Management
$66,997–$83,803 year
Hybrid · Princeton, New Jersey, United States
Job Summary
Senior Associate in R&D Quality and Risk Management at Acadia Pharmaceuticals. Lead KPIs for quality metrics, support QRM regulatory framework, develop training materials for GCP/GLP/GvP, guide study-specific teams through Veeva QMS for Deviation and CAPA, contribute to process improvements in R&D and GMP spaces, participate in IT-enabled trial management, and support Health Authority inspections. Emphasis on implementing and validating quality processes, data-driven decision making, and cross-functional collaboration in a regulated clinical development environment. Requires collaboration with QRM and clinical study teams, knowledge of ICH GCP guidelines, and ability to travel occasionally. Hybrid work model with Princeton office presence three days per week.
Required Qualifications
- Bachelor’s degree in life sciences, neuroscience, psychology, biochemistry, engineering, Quality (and/or Risk) Management, Clinical Pharmacology or related field
- Targeting 2+ years of Pharmaceutical/Health Care experience in a R&D regulated environment including some experience in Risk-Based Quality Management or R&D Quality Assurance systems and Health Authority regulations (e.g. ICH E6; FDA 21 CFR)
Additional Requirements
- Ability to travel in exceptional cases.
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