STEM Content Analyst - Regulatory Intelligence

Roles & Responsibilities
• Monitor global and regional regulatory updates from FDA, EMA, WHO, and national health authorities
• Interpret and contextualize regulatory changes across Pharmaceuticals, Biologics, Advanced Therapies, Medical Technologies & Digital Health
• Convert regulatory updates into structured content for Cortellis Regulatory Intelligence country modules
• Analyze legislation, guidance documents, and consultations for lifecycle impact
• Validate and review AI-generated regulatory content for accuracy and compliance
• Collaborate with global editorial, product, and technology teams
• Coordinate with external consultants and local regulatory experts
• Support initiatives related to AI-assisted workflow optimization, content harmonization, and quality assurance

Qualification
• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Chemistry, or Regulatory Affairs

Experience
• 3–5 years in Regulatory Affairs, Regulatory Intelligence, Pharmaceutical Development, or Quality/Compliance roles

Skills
• Strong understanding of global regulatory frameworks
• Excellent analytical, writing, and editorial skills
• Fluency in English
• (Preferred) Experience developing regulatory intelligence content, knowledge of submission lifecycle management, familiarity with AI/ML-enabled editorial tools, understanding of quality management systems (QMS)

About the Organization
Clarivate is a global leader in providing trusted insights and analytics to accelerate the pace of innovation. Its Life Sciences division offers intelligence solutions that help organizations navigate complex regulatory landscapes and make informed decisions efficiently.