Freelance Clinical Documentation Reviewer — Pharmaceuticals (US)

Uber AI Solutions; United States; Remote; USD 30,000 - 48,000; Full time

Job summary

Uber AI Solutions is seeking experienced pharmaceutical industry professionals to train and evaluate AI systems by reviewing, labeling, and assessing technical content from development, manufacturing, quality, and regulation of medicines. Remote, independent work with strong judgment.

You will annotate technical content, evaluate AI outputs for accuracy, spot errors, and follow detailed guidelines precisely, contributing to quality checks and guideline improvements with the project team.

Qualifications

• Significant experience in the pharmaceutical/biopharmaceutical industry.
• Strong knowledge of the standards and regulatory environment applicable to the work.
• Excellent attention to detail and habit of checking your own work.
• Proven ability to follow long or nuanced written instructions accurately.
• Clear, well-structured written communication justifying judgments.
• Comfortable working independently and managing time remotely.

Responsibilities

• Review and annotate technical and scientific content from pharmaceutical and biopharmaceutical industry work.
• Evaluate AI-generated outputs for accuracy, completeness, and consistency.
• Spot errors, gaps, and inconsistencies, and explain your reasoning clearly.
• Follow detailed annotation guidelines precisely and apply them consistently.
• Work with the project team to clarify edge cases and improve guidelines.
• Take part in quality checks on your own work and on the work of others.

Skills

Pharmaceutical industry experience

Regulatory knowledge

Attention to detail

Following instructions

Clear written communication

Job description

We're looking for experienced pharmaceutical industry professionals to help train and evaluate AI systems. You'll apply your professional judgment to review, label, and assess technical content from the development, manufacture, quality, and regulation of medicines. You'll also give structured feedback on AI-generated outputs. Your industry expertise is the asset.

What you'll do

• Review and annotate technical and scientific content from pharmaceutical and biopharmaceutical industry work
• Evaluate AI-generated outputs for accuracy, completeness, and consistency
• Spot errors, gaps, and inconsistencies, and explain your reasoning clearly
• Follow detailed annotation guidelines precisely and apply them consistently
• Work with the project team to clarify edge cases and improve guidelines
• Take part in quality checks on your own work and on the work of others

About you

• Significant professional experience working in the pharmaceutical or biopharmaceutical industry, such as at a manufacturer, drug developer, contract organization, or in a regulatory or quality function
• Strong working knowledge of the standards and regulatory environment that apply to your area of work
• Excellent attention to detail and a habit of checking your own work
• Proven ability to follow written instructions exactly, including when they are long or nuanced
• Clear written communication, including the ability to justify your judgments
• Comfortable working independently and managing your own time in a remote setting

Please note:

This role is focused on pharmaceutical industry work. It is not a clinical, hospital, or retail pharmacy role.