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Alpheva AI offers remote, project-based clinical-operations expert work evaluating AI-assisted clinical tasks. The role emphasizes balancing timelines, quality, and participant protection, with asynchronous collaboration across our research teams.
Experts with 8+ years in sponsor/CRO/site operations will evaluate AI recommendations, ensure ICH-GCP compliance, and contribute to inspection readiness. Flexible hours and project-matching opportunities are provided.
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.
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.