Legal AI Training Jobs
Legal AI training jobs for lawyers, paralegals and law students: draft, review and grade legal answers written by AI. Bar admission and degree requirements are listed.
$100/hr
Typical $80–$125/hr across 133 roles with listed pay
By field
Job listings 5
Medicine & Healthcare Clear all
DataAnnotationHealthcare Compliance SpecialistMedicine & Healthcare / Law · today WorldwideUp to $125/hrApply
About this role
The person drafts prompts about healthcare compliance, evaluates AI answers against current rules, and writes corrected guidance tied to governing regulations. The work suits someone with hands-on healthcare compliance, privacy, or regulatory experience and familiarity with HIPAA.
What you'd do
- Rate and critique AI answers
- Write prompts and tasks
- Write ideal answers
Requirements
- No degree required
- Hands-on healthcare compliance, privacy, or regulatory experience
- Familiarity with HIPAA and healthcare regulatory frameworks
- Clear written English
- Language: EN
Full description
- Platform
- DataAnnotation
- Pay rate
- Up to $125/hr
- Eligibility
- Worldwide
- Expertise
- Medicine & Healthcare, Law
- Level
- Mid-level
- Posted
- today
EthosExpert Opportunity - Clinical Research Officer ($100/hr, up to $2,000/week)Medicine & Healthcare / Biology & Life Sciences / Law · today
India$100/hrApply
About this role
Create, evaluate, and refine AI-generated clinical research documents, spreadsheets, and slide decks, including study reports and regulatory materials. This suits an experienced clinical research, biomedical science, or pharmaceutical/regulatory affairs professional with direct document-authoring or review experience.
What you'd do
- Rate and critique AI answers
- Write ideal answers
Requirements
- 5+ years of experience
- Direct experience authoring or reviewing clinical study reports, protocol synopses, or regulatory dossier modules for a pharmaceutical, biotech, or CRO organization
- Deep familiarity with ICH-GCP standards and FDA/EMA regulatory expectations
- Expert-level document, spreadsheet, and slide craftsmanship
- Excellent written communication and attention to detail
- Language: EN
Commitment
- 5–20 hours a week
- Flexible schedule
- Ongoing
Full description
- Platform
- Ethos
- Pay rate
- $100/hr
- Eligibility
- India
- Expertise
- Medicine & Healthcare, Biology & Life Sciences, Law
- Level
- Expert
- Posted
- today
EthosExpert Opportunity - Clinical Research Associate ($100/hr, up to $2,000/week)Medicine & Healthcare / Biology & Life Sciences / Law · todayIndia$100/hrApply
About this role
The person creates, evaluates, and refines AI-generated clinical research and regulatory documents, spreadsheets, and slide decks. The work suits an experienced clinical research associate with direct pharmaceutical, biotech, or CRO experience and strong knowledge of clinical and regulatory standards.
What you'd do
- Rate and critique AI answers
- Write ideal answers
Requirements
- 5+ years of experience
- Direct experience authoring or reviewing specified clinical research or regulatory documents for a pharmaceutical, biotech, or CRO organization
- Deep familiarity with ICH-GCP standards and FDA/EMA regulatory expectations
- Expert-level document, spreadsheet, and slide craftsmanship
- Excellent written communication and attention to detail
- Language: EN
Commitment
- 5–20 hours a week
- Flexible schedule
Full description
- Platform
- Ethos
- Pay rate
- $100/hr
- Eligibility
- India
- Expertise
- Medicine & Healthcare, Biology & Life Sciences, Law
- Level
- Expert
- Posted
- today
EthosExpert Opportunity - Head of Regulatory Affairs ($100/hr, up to $2,000/week)Medicine & Healthcare / Law / Writing & Editing · todayIndia$100/hrApply
About this role
Create, evaluate, and refine AI-generated clinical and regulatory documents, spreadsheets, and slide decks, including study reports and regulatory dossier materials. This suits senior regulatory affairs professionals with at least five years of relevant experience and direct pharmaceutical, biotech, or CRO document experience.
What you'd do
- Rate and critique AI answers
- Write ideal answers
Requirements
- 5+ years of experience
- Direct experience authoring or reviewing clinical study reports, protocol synopses, or regulatory dossier modules for a pharmaceutical, biotech, or CRO organization
- Deep familiarity with ICH-GCP standards and FDA/EMA regulatory expectations
- Expert-level document, spreadsheet, and slide craftsmanship
- Excellent written communication and attention to detail
- Language: EN
Commitment
- 5–20 hours a week
- Flexible schedule
- Ongoing
Full description
- Platform
- Ethos
- Pay rate
- $100/hr
- Eligibility
- India
- Expertise
- Medicine & Healthcare, Law, Writing & Editing
- Level
- Expert
- Posted
- today
EthosExpert Opportunity - Regulatory Affairs Specialist ($100/hr, up to $2,000/week)Medicine & Healthcare / Biology & Life Sciences / Law · todayIndia$100/hrApply
About this role
Create, evaluate, and refine AI-generated clinical and regulatory documents, spreadsheets, and slide decks, including study reports, regulatory materials, and medical affairs presentations. This suits an experienced regulatory affairs specialist with pharmaceutical, biotech, or CRO experience and strong document, spreadsheet, and slide skills.
What you'd do
- Rate and critique AI answers
- Write ideal answers
Requirements
- 5+ years of experience
- Direct experience authoring or reviewing clinical study reports, protocol synopses, or regulatory dossier modules for a pharmaceutical, biotech, or CRO organization
- Deep familiarity with ICH-GCP standards and FDA/EMA regulatory expectations
- Expert-level document, spreadsheet, and slide skills
- Excellent written communication and attention to detail
- Language: EN
Commitment
- 5–20 hours a week
- Flexible schedule
Full description
- Platform
- Ethos
- Pay rate
- $100/hr
- Eligibility
- India
- Expertise
- Medicine & Healthcare, Biology & Life Sciences, Law
- Level
- Expert
- Posted
- today
Showing 1-5 of 5 positions