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OpenTrain AIFor AI Companies

Clinical Pharmacology AI Training Expert

Use your clinical pharmacology expertise to create rigorous PK/PD datasets, dosing rationale, and AI evaluation tasks. This remote contract role pays $120-$170 per hour and requires 20-25 hours weekly.

OpenTrain AI

Medical & Health

Remote Hourly · $120–$170/hr

$120–$170/hr

Compensation

3 countries

Eligibility

Entry

Experience

Aug 20, 2026

Posted

Open to applicants in

United States Canada France

Interested in this role?

Create a free OpenTrain account and apply in minutes.

About OpenTrain

OpenTrain is the #1 platform for finding and building careers in AI training and data labeling. OpenTrain AI recruits specialists for projects that help shape how advanced AI systems understand and produce expert-level work.

As an OpenTrain contractor, you can build a professional AI training portfolio, discover projects aligned with your expertise, and apply in minutes through a free account.

About Clinical Pharmacology AI Training

AI training is the human side of building artificial intelligence. Expert contributors create examples, write prompts, evaluate model responses, and develop scoring standards that help AI systems produce more accurate and reliable results.

In this role, your clinical pharmacology judgment will help assess whether AI-generated work is clinically plausible, internally consistent, and appropriately connected across pharmacokinetics, pharmacodynamics, efficacy, and safety.

The Role

OpenTrain is seeking a Clinical Pharmacology AI Training Expert to create and evaluate clinically plausible pharmacology content for AI training workflows. You will simulate PK and PD datasets, dosing and escalation regimens, exposure-response relationships, and bioanalytical reports.

Your work will ensure that dose rationale and concentration data reconcile with efficacy and safety outputs. You will also author clinical pharmacology tasks and develop prompts, golden outputs, and rubrics that measure an AI agent's ability to perform this work.

  • Contract role with part-time availability
  • Remote work
  • Open to candidates in the United States or Canada according to the role description
  • Structured location eligibility also lists France
  • Minimum availability of 20-25 hours per week
  • Preferred availability of 30 or more hours per week
  • Default commitment of 40 hours per week
  • Pay range of $120-$170 USD per hour

What You'll Do

You will produce expert-level clinical pharmacology materials suitable for review and use in AI training workflows. Work from protocols and statistical analysis plans to create realistic, clinically coherent data and evaluation content.

  • Build PK and PD datasets for clinical data rooms
  • Create realistic bioanalytical reports
  • Develop clinically plausible dosing and escalation regimens
  • Model exposure-response relationships
  • Write dose-selection rationale
  • Author drug concentration and response sections
  • Create drug-drug and drug-disease interaction content
  • Develop prompts, golden outputs, and evaluation rubrics
  • Produce pharmacology data suitable for expert review
  • Evaluate whether pharmacology reconciles with efficacy and safety outputs

Required Qualifications

This role requires substantial professional clinical pharmacology experience and the ability to apply rigorous PK/PD judgment to pre-market drug development programs. Candidates must be able to create technically credible content and identify whether dose, concentration, efficacy, and safety information is consistent.

  • At least five years of professional experience in clinical pharmacology
  • Hands-on PK/PD analysis experience
  • Experience with dose selection and escalation
  • Experience with exposure-response analysis
  • Experience supporting pre-market Phase 1-3 programs as a clinical pharmacologist
  • PharmD, PhD in pharmacology or pharmacokinetics, MD, or equivalent education
  • Ability to produce clinically rigorous work that reconciles pharmacology with efficacy and safety outputs
  • Ability to author dose rationale and drug interaction content
  • Ability to work from protocols and statistical analysis plans

Helpful Background

The following experience is valuable for this project and may help you contribute effectively to realistic clinical pharmacology training materials.

  • First-in-human program experience
  • Familiarity with clinical protocols
  • Familiarity with statistical analysis plans
  • Experience authoring drug interaction content

Why Work in AI Training

AI training and data labeling are rapidly expanding areas of tech work, with projects spanning expert evaluation, document creation, model feedback, and structured annotation. Specialists can contribute directly to how cutting-edge AI systems perform in demanding professional fields.

Remote, flexible contract work can fit around other professional commitments while giving you a way to build a durable portfolio of AI training experience.

How to Apply Through OpenTrain

Create a free OpenTrain account, build a profile that reflects your clinical pharmacology background, and apply in minutes. Your profile can help demonstrate credible experience across AI training opportunities and support a longer-term career in the field.

  • Review the role and confirm your availability
  • Highlight your clinical pharmacology, PK/PD, and drug development experience
  • Show relevant experience with protocols, statistical analysis plans, and interaction content
  • Apply through OpenTrain

Ready to apply?

Create a free OpenTrain account and apply for this role in minutes.

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