Clinical Trials Specialist - Fully Remote | Upto $50/hr Part-time

mercor; San Francisco (CA); Hybrid; CAD 81,000 - 115,000; Part time

Job summary

Mercor is seeking a part-time contractor for Pharma & Clinical Trials — Visual Document Understanding. This remote role requires 15–20 hours per week.

You will evaluate AI models on pharma documents, author grounded tasks with clear rubrics, review outputs for accuracy, and collaborate with domain experts to ensure dataset relevance. Independent, deadline-driven work style is essential.

Qualifications

• Must have expertise in Pharma & Clinical Trials domain.
• Must have strong understanding of visual document processing.

Responsibilities

• Evaluate AI models on visual document understanding in the Pharma & Clinical Trials domain.
• Author complex, grounded tasks with clear ground-truth outputs and objective rubrics.
• Review and improve AI model outputs for accuracy and alignment with domain principles.
• Collaborate with subject matter experts to ensure consistency and relevance across datasets.
• Work independently and asynchronously to meet deadlines while enhancing AI model performance.

Skills

Pharma & Clinical Trials

Visual document processing

Job description

About the job

Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark , General Catalyst , Peter Thiel , Adam D'Angelo , Larry Summers , and Jack Dorsey .

Position

Pharma & Clinical Trials — Visual Document Understanding

Type: Contract

Compensation: $50/hour

Location: Remote

Commitment: 15–20 hours/week

Role Responsibilities

• Evaluate AI models on visual document understanding in the Pharma & Clinical Trials domain.
• Author complex, grounded tasks with clear ground-truth outputs and objective rubrics.
• Review and improve AI model outputs for accuracy and alignment with domain principles.
• Collaborate with subject matter experts to ensure consistency and relevance across datasets.
• Work independently and asynchronously to meet deadlines while enhancing AI model performance.

Qualifications

• Must-Have: Expertise in Pharma & Clinical Trials domain.
• Must-Have: Strong understanding of visual document processing.

Resources & Support

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