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Job Description

Evaluate clinical-trial planning, site operations, protocol execution, monitoring, and inspection-readiness decisions across drug-development programs. Review AI-generated recommendations for feasibility, patient safety, data integrity, protocol compliance, and sponsor or CRO oversight. Identify operational assumptions, missing documentation, escalation gaps, and site-management decisions that conflict with ICH-GCP practice. Provide clear corrections that reflect how experienced clinical-operations leaders balance timelines, quality, and participant protection. Remote, project-based contract work. Scope and hours depend on project matching; the listed hourly range applies to matched work.

Why Apply

• Expert-level compensationEarn $130 - $200/hr for work that values your professional judgment.
• Flexible remote workContribute asynchronously around your existing professional commitments.
• Meaningful model impactHelp advanced AI systems reason more accurately in healthcare & life sciences.
• Focused projectsAccept only the opportunities that fit your experience and availability.

Responsibilities

• Evaluate advanced domain tasks and AI-generated responses for factual accuracy and professional judgment.
• Apply current standards, methods, and risk considerations from healthcare & life sciences.
• Document errors, edge cases, and the reasoning behind an ideal response.
• Collaborate asynchronously with Alpheva's research and evaluation teams.

Required Qualifications

• 8+ years in sponsor, CRO, or site-level clinical operations
• Deep knowledge of ICH-GCP, trial monitoring, site management, and protocol-deviation handling
• Clinical program leadership or inspection-readiness experience preferred

Company Description

Alpheva AI builds the expert data, evaluations, and real-world environments that help frontier AI systems become more capable and reliable. We partner with experienced professionals whose judgment can teach models how high-quality work is actually done.