Pharmacovigilance Safety Evaluator

AuraOne, Inc.; United States; Remote; USD 34,000 - 69,000; Full time

Job summary

AuraOne, Inc. is seeking a Pharmacovigilance Safety Evaluator for a remote, contractor role. You will review model outputs against a rubric, label edge cases, and provide structured feedback to retrain the system. The work requires clear written reasoning and reliable weekly availability.

Applicants must be authorized to work from the United States. This is a contractor position with remote, US-eligible work and no full-time commitments.

Qualifications

• Prior evaluation or annotation experience in pharmacovigilance safety evaluation.
• Ability to apply long-form rubrics consistently across batches.
• Clear written rationale citing rubric clauses being applied.
• Strong attention to detail and flagging when a prompt is the problem.
• Reliable async availability for at least 10 hours per week.

Responsibilities

• Evaluate pharmacovigilance safety evaluation model outputs against a versioned rubric and assign severity tags for assignments.
• Compare paired responses and pick the stronger answer with a written rationale.
• Label hallucinations, instruction-following failures, and unsafe content with structured tags.
• Capture ambiguous prompts and route them back to the program team for rubric updates.
• Maintain reviewer-quality scores by calibrating against gold-standard examples each week.
• Document recurring failure modes so the modeling team can target them in the next training run.

Skills

Model evaluation

Rubric annotation

Severity tagging

Inter-rater calibration

Pharmacovigilance

Clinical review

Patient safety

Guideline reasoning

Pharmacovigilance safety

Job description

Pharmacovigilance Safety Evaluator is a remote evaluation track for reviewing pharmacovigilance safety evaluation prompts and responses against AuraOne's quality rubric. Reviewers compare paired outputs, label edge cases, and write the kind of structured feedback the modeling team can use to retrain.

Why this role matters

AI data reviewers help turn pharmacovigilance safety evaluation outputs into auditable labels, rationales, and regression cases for AuraOne Human Data.

Responsibilities

• Evaluate pharmacovigilance safety evaluation model outputs against a versioned rubric and assign severity tags for Pharmacovigilance Safety Evaluator assignments.
• Compare paired responses and pick the stronger answer with a written rationale.
• Label hallucinations, instruction-following failures, and unsafe content with structured tags.
• Capture ambiguous prompts and route them back to the program team for rubric updates.
• Maintain reviewer-quality scores by calibrating against gold-standard examples each week.
• Document recurring failure modes so the modeling team can target them in the next training run.

Qualifications

• Prior evaluation, annotation, or human-rater experience on pharmacovigilance safety evaluation or adjacent content for Pharmacovigilance Safety Evaluator work.
• Comfort applying multi-page rubrics consistently across long batches.
• Clear written reasoning that names the issue and the rubric clause being applied.
• Strong attention to detail and the ability to flag when a prompt itself is the problem.
• Reliable async availability for at least 10 hours per week.

Example tasks

• Compare two pharmacovigilance safety evaluation model responses to the same prompt and pick the stronger one with rationale.
• Tag an unsafe response with the correct policy category and severity.
• Audit a 50-row batch for rubric consistency and report drift to the program lead.
• Propose a rubric clarification after spotting a recurring failure mode.

Nice to have

• Background in linguistics, content moderation, or trust & safety review.
• Experience with inter-rater agreement metrics and calibration cycles.
• Domain expertise that lets you spot subject-matter errors automated checks miss.

Skills

• Model output evaluation
• Rubric-based annotation
• Severity tagging
• Inter-rater calibration
• Pharmacovigilance Safety evaluation
• Clinical review
• Patient safety
• Guideline reasoning
• Pharmacovigilance

Work model

Remote — US-eligible. Remote · Independent specialist contractor. Employment type: CONTRACTOR. Applicants must be authorized to work from US.

Compensation

Hourly rate confirmed after the interview process.

Application process

Apply through AuraOne's specialist intake for role-specific routing and review. Final project scope, schedule, and contractor terms are confirmed before placement.