Remote MSL: AI Medical Content Quality Expert

Alignerr Corp.

España

Remote

EUR 69,000 - 103,000

Full time

26 hours ago
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Benefits offered by this job

Fully remote
Flexible schedule
Global collaboration

Job summary

Alignerr is seeking an experienced Medical Science Liaison to assist in evaluating AI-trained biomedical and healthcare content. You will ensure scientific accuracy, clear communication, and appropriate interpretation of clinical data within AI outputs.

This remote, hourly-contract role offers 10–40 hours per week, flexible scheduling, and global collaboration. You will review trial data, safety profiles, and regulatory materials, delivering structured feedback to improve AI behavior in

Qualifications

  • Experience interpreting clinical publications, trial data, and regulatory documents.
  • Ability to evaluate AI-generated clinical content for accuracy and clarity.
  • Provide structured, expert feedback on medical content for AI outputs.
  • Experience working remotely and asynchronously is a plus.

Responsibilities

  • Review and evaluate AI-generated medical and clinical content for accuracy, clarity, and appropriateness
  • Identify errors, unsupported claims, or misleading representations of clinical evidence
  • Validate that trial data, safety profiles, and regulatory materials are accurately represented
  • Provide structured, expert feedback to improve AI outputs across medical and life-science domains
  • Work independently and asynchronously on your schedule

Skills

Medical affairs background
HCP engagement experience
Evidence interpretation (publications,

Education

Advanced degree in life-science/medical field (PharmD/MD/PhD)

Job description

Alignerr is seeking an experienced Medical Science Liaison to assist in evaluating AI-trained biomedical and healthcare content. You will ensure scientific accuracy, clear communication, and appropriate interpretation of clinical data within AI outputs.

This remote, hourly-contract role offers 10–40 hours per week, flexible scheduling, and global collaboration. You will review trial data, safety profiles, and regulatory materials, delivering structured feedback to improve AI behavior in

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