Regulatory Affairs Expert - Remote
YO AI Labs · Anywhere, IL
CONTRACT
Remote
Posted Aug 10, 2026
Job Description
Job Title: Regulatory Affairs Specialist
Location: Remote
Job Type: Contract
Job Description
We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating regulatory documentation. The role involves assessing clinical documents, ensuring compliance with regulatory guidelines, identifying inconsistencies, and providing clear, evidence-based feedback to improve AI-generated regulatory content.
Key Responsibilities
- Review and evaluate clinical and regulatory documentation.
- Assess regulatory submissions and responses for accuracy and compliance.
- Ensure adherence to ICH guidelines and CTD/eCTD requirements.
- Identify regulatory risks, inconsistencies, and unsupported claims.
- Prepare structured, guideline-based written feedback.
Required Qualifications
- 5+ years of Regulatory Affairs experience in the pharmaceutical, biotech, or CRO industry.
- Experience with clinical submissions, regulatory documentation, and health authority interactions.
- Strong knowledge of ICH guidelines and CTD/eCTD structure.
- Excellent analytical, critical thinking, and written communication skills.
- Degree in Life Sciences, Pharmacy, Medicine, or a related field.
Location: Remote
Job Type: Contract
Job Description
We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating regulatory documentation. The role involves assessing clinical documents, ensuring compliance with regulatory guidelines, identifying inconsistencies, and providing clear, evidence-based feedback to improve AI-generated regulatory content.
Key Responsibilities
- Review and evaluate clinical and regulatory documentation.
- Assess regulatory submissions and responses for accuracy and compliance.
- Ensure adherence to ICH guidelines and CTD/eCTD requirements.
- Identify regulatory risks, inconsistencies, and unsupported claims.
- Prepare structured, guideline-based written feedback.
Required Qualifications
- 5+ years of Regulatory Affairs experience in the pharmaceutical, biotech, or CRO industry.
- Experience with clinical submissions, regulatory documentation, and health authority interactions.
- Strong knowledge of ICH guidelines and CTD/eCTD structure.
- Excellent analytical, critical thinking, and written communication skills.
- Degree in Life Sciences, Pharmacy, Medicine, or a related field.
Additional Details
- State
- Illinois
- Country
- US
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