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Verista
Csa Consultant Pv Clinical Ra
Remote · King of Prussia, Remote · Full time · Mid level
$70.5k–$118k / year
About the role
Support GxP compliance activities across Pharmacovigilance, Clinical, and Regulatory Affairs systems. Ensure systems meet regulatory and internal compliance requirements.
What you’ll do
• Provide CSA/CSV expertise across PV, Clinical, Regulatory platforms. • Support system implementations and upgrades from compliance perspective. • Develop and review validation deliverables. • Oversee validation readiness and lifecycle documentation. • Conduct compliance reviews and support change control activities.
What you’ll bring
• 5-8 years supporting GxP systems in PV, Clinical, or Regulatory domains. • Strong understanding of CSA principles and CSV processes. • Experience authoring validation documentation. • Knowledge of FDA, EMA, ICH regulations and data integrity. • Strong communication and independent work skills.
Life at Verista
High growth, people-focused culture with competitive pay and benefits. Includes insurance, 401(k), PTO, tuition reimbursement, and social activities.
About Verista
Verista provides innovative solutions and services to life science clients to empower informed decision-making and improve healthcare outcomes.