Medical Writer (Pharmaceutical)

AuraOne; United States; Remote; USD 103,000 - 152,000; Full time

Job summary

AuraOne is seeking a Medical Writer (Pharmaceutical) for a remote contractor role to evaluate AI outputs that touch pharma. You will review clinical reasoning, dosing logic, and guideline adherence, flag patient-safety issues, and document corrected reasoning for the modeling team.

Qualifications include an active pharma license or board certification and hands-on clinical experience reading patient cases. You will apply multi-page rubrics consistently, cite guidelines, and maintain reviewer

Qualifications

• Active or recent pharma license or board certification.
• Hands-on clinical experience reading patient cases.
• Experience applying multi-page rubrics.
• Clear written reasoning citing guidelines or standard of care.
• Reliable async availability for at least 10 hours/week.

Responsibilities

• Review AI outputs against pharma guidelines and standard of care.
• Grade differential reasoning, dosing, and red-flag handling.
• Flag patient-safety issues with severity tags.
• Capture corrected clinical reasoning for training.
• Adjudicate disputed cases using current guidelines.
• Maintain reviewer-quality scores in weekly calibrations.

Skills

Clinical reasoning

Guideline review

Patient-safety assessment

Structured clinical writing

Pharma

Healthcare

Education

Active pharma license or board certification

Job description

Category: Medical & Clinical AI · Pay: $75–$110 / hr · Location: Remote — US-eligible · Contractor

Medical Writer (Pharmaceutical) is a remote clinical-review track for evaluating AI outputs that touch pharma. Reviewers grade differential reasoning, dosing logic, and guideline adherence; flag patient-safety issues; and document the corrected clinical reasoning so the modeling team can close the gap.

Why this role matters

Pharma AI is only useful if a credentialed clinician would sign their name to the output. AuraOne uses licensed and credentialed reviewers to set the bar for clinical reasoning, dosing, and guideline adherence in regulated workflows.

Responsibilities

• Review AI outputs against current pharma clinical guidelines and standard of care for Medical Writer (Pharmaceutical) assignments.
• Grade differential reasoning, dosing, and red-flag handling on a structured rubric.
• Flag patient-safety issues with severity tags that match clinical-incident taxonomies.
• Capture the corrected clinical reasoning so the modeling team can train on it.
• Adjudicate disputed cases against published evidence or specialty guidelines.
• Maintain reviewer-quality scores in weekly inter-rater calibration cycles.

Qualifications

• Active or recent license / board certification in pharma or an adjacent specialty for Medical Writer (Pharmaceutical) work.
• Hands‑on clinical experience reading patient cases and writing structured assessments.
• Comfort applying multi‑page rubrics consistently across long batches.
• Clear written reasoning that cites guidelines, evidence, or standard of care.
• Reliable async availability for at least 10 hours per week.

Example tasks

• Grade a model's differential‑diagnosis reasoning on a pharma case and write a 2‑3 sentence assessment.
• Flag a dosing miscalculation with the right severity tag and corrected dose.
• Adjudicate a disputed case between two reviewers using current specialty guidelines.
• Audit a 25‑case batch for rubric consistency and report drift to the program lead.

Nice to have

• Prior work as a guideline reviewer, peer reviewer, or clinical educator.
• Familiarity with AI‑assisted clinical decision support and its failure modes.
• Bilingual clinical experience for non‑English patient cases.

Skills

• Clinical reasoning
• Guideline review
• Patient‑safety assessment
• Structured clinical writing
• Pharma
• Healthcare

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.