Job Description:
• Review and evaluate HCP- and patient-facing Voice AI interactions for regulatory compliance.
• Assess alignment with approved labeling, regulatory guidance, and promotional boundaries.
• Identify regulatory risk, ambiguity, or precedent concerns in AI-driven interactions.
• Apply real-world regulatory judgment to distinguish material risk from low-risk deviations.
• Score interactions using defined regulatory rubrics and provide clear, actionable feedback.
• Flag potential regulatory compliance risks and areas requiring escalation or mitigation.
Requirements:
• 3–10+ years of experience in Pharmaceutical Regulatory Affairs
• Direct involvement in MLR/PRC review processes as a Regulatory contributor or decision-maker
• Strong understanding of promotional regulations, labeling, and regulatory risk assessment
• Ability to make clear, defensible regulatory judgment calls
• Strong written communication skills
• Fluency in English
• Reliable access to a computer and high-speed internet
Benefits:
• Flexible schedule, typically averaging 10–15 hours per week
• Opportunity for expansion into a full-time role based on performance and organizational needs
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