0024V Computer System Assurance (CSA) Consultant – PV/Clinical/Regulatory Affairs

0024V Computer System Assurance (CSA) Consultant – PV/Clinical/Regulatory Affairs Please contact Amanda Mazza, [email protected] We are seeking an experienced Computer System Assurance (CSA) Consultant to support GxP compliance activities across Pharmacovigilance (PV), Clinical, and Regulatory Affairs systems. This role will work closely with Quality, IT, and business stakeholders to ensure systems are implemented, maintained, and operated in compliance with applicable regulations and internal procedures. Key Responsibilities • Provide CSA / CSV subject matter expertise across PV, Clinical, and Regulatory Affairs platforms • Support system implementations, enhancements, integrations, upgrades, and data migrations from a compliance perspective • Develop and review validation deliverables including Validation Plans, Risk Assessments, Traceability Matrices, and Validation Summary Reports • Review and approve lifecycle documentation (URS, specifications, test plans, test summaries) in alignment with ALCOA+ and Good Documentation Practices • Oversee validation readiness and ensure prerequisites are met prior to formal testing • Support change control, configuration management, and release activities • Partner with Quality, System Owners, and Business Process Owners to ensure ongoing compliance • Provide guidance on CSA-based, risk-driven validation approaches Required Experience & Qualifications • 5–8 years of hands-on experience supporting GxP systems in Pharmacovigilance, Clinical, Regulatory Affairs, or a combination of these domains • Hands-on experience supporting GxP systems in Pharmacovigilance, Clinical, Regulatory Affairs, or a combination of these domains • Strong understanding of CSA principles, CSV, and SDLC processes • Experience authoring and/or reviewing validation documentation • Working knowledge of GxP regulations (e.g., FDA, EMA, ICH) and data integrity expectations • Ability to work independently in a fast-paced, matrixed environment • Strong communication skills and comfort interacting with Quality and business stakeholders Preferred Experience • Experience with enterprise platforms supporting PV, Clinical, or Regulatory operations • Prior role as a Validation SME, CSA Lead, or Compliance Consultant • Familiarity with electronic quality systems, change management tools, or application lifecycle management platforms LOCATION Remote EMPLOYMENT Competitive C2C or W2 Contractor – 17-month assignment Powered by JazzHR Remote About the Company: Two River Consulting Partners Apply tot his job