Clinical Data Manager (CDM)

Role Overview

Bring your pharmaceutical and clinical trial knowledge to a specialized visual-document review initiative. The work centers on building strong assessment tasks and benchmark materials that are accurate, objective, and useful for evaluation.

What You Will Be Doing

• Create advanced, domain-specific tasks from pharmaceutical and clinical trial documents.
• Examine visual documents and define expected outputs that are clear and evidence-based.
• Build objective grading rubrics with measurable criteria for success.
• Check task quality to keep outputs accurate, consistent, and relevant to the domain.
• Contribute to the creation of structured benchmarks for document understanding and instruction-following evaluation.

Who We Are Looking For

• Experienced professionals with strong exposure to pharmaceuticals, drug development, clinical research, or clinical trials.
• Solid knowledge of clinical trial records, regulatory documents, and research processes.
• Ability to design precise, evidence-backed tasks with unambiguous expected results.
• Strong analytical ability and a sharp eye for detail.
• Excellent written communication skills and the capacity to work in a structured evaluation format.

Role Details

This is a remote, part-time contract engagement. The work is project-based and ongoing.

Compensation is $50 per hour.

Application Process

• Use the Easy Apply option to submit your application.
• Only shortlisted candidates will be contacted with the next steps.