We are looking for a Regulatory Intelligence Content Analyst to join our Life Sciences Regulatory Intelligence team. The ideal candidate will bring strong regulatory knowledge across pharmaceuticals, biologics, advanced therapies, and related life sciences domains, combined with the ability to deliver high quality, accurate, and timely regulatory intelligence.

You will be responsible for monitoring global regulatory changes, interpreting complex requirements, and ensuring the accuracy and integrity of country specific content within our AI-enhanced editorial production environment. Your ability to combine regulatory expertise with advanced content production tools will be essential to maintaining Cortellis Regulatory Intelligence (CRI)’s accuracy, credibility, and operational efficiency.

About You – experience, education, skills, and accomplishments  

• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Chemistry, Regulatory Affairs, or another relevant field.
• Minimum 3–5 years of experience in regulatory affairs, regulatory intelligence, pharmaceutical development, quality compliance, or related life sciences roles.
• Strong understanding of global and regional health authority frameworks (e.g., FDA, EMA, WHO, national Ministries of Health).
• Ability to interpret and synthesize regulatory requirements related to pharmaceuticals, biologics, advanced therapies, medical technologies, or digital health.
• Experience assessing legislation, guidance documents, and regulatory updates with strong analytical and contextual judgment.
• Familiarity with AI‑assisted editorial workflows or experience validating AI‑generated outputs.
• Excellent written communication, attention to detail, and editorial precision.
• Ability to work effectively with global, cross‑functional, and remote teams.
• Fluency in English; additional languages are an asset.

It would be great if you also had…

• Prior experience developing regulatory intelligence or structured regulatory content.
• Knowledge of regulatory lifecycle management (submissions, approvals, post‑approval changes).
• Experience engaging with external consultants or local regulatory experts.
• Understanding of quality management principles, compliance frameworks, and information classification.
• Insight into AI/ML‑enabled content production or digital transformation initiatives in regulatory affairs.

What will you be doing in this role?

• Monitor global and regional regulatory developments from competent authorities, Ministries of Health, and international regulatory bodies.
• Interpret and contextualize complex regulatory updates across pharmaceuticals, biologics, medical technologies, digital health, and quality/manufacturing compliance.
• Transform regulatory changes into structured, high‑quality intelligence for CRI’s country modules and internal databases.
• Conduct in‑depth analysis of legislation, guidance, and consultations, identifying impacts on submissions, approvals, and lifecycle management.
• Collaborate with AI‑enabled content production workflows to enrich content, improve efficiency, and apply expert oversight for quality assurance.
• Coordinate with external consultants and local experts to ensure accuracy and precision in country‑level regulatory information.
• Communicate key regulatory insights to internal teams, editorial partners, and customer‑facing functions.
• Support cross‑functional initiatives including:
  • AI‑assisted workflow optimization
  • Product and feature enhancements
  • Quality assurance and compliance improvements
  • Global content harmonization

About the Team   

As part of the Regulatory Market Access organization, the Regulatory Intelligence team is responsible for curating high‑quality global regulatory content across the full lifecycle of pharmaceutical and life sciences products. The team works closely with Product, Technology, Customer Care, Product Specialists/Account Manager and external experts to deliver trusted regulatory insights that support compliance, market access, and strategic decision‑making. Our team is geographically distributed across France, Malaysia, India, Serbia, Spain, and other global locations.

Hours of Work  

Hybrid work mode (Monday to Friday). The work timing is 8-9AM / 5-6PM IST.

Location: Hybrid

At Clarivate, we are committed to providing equal employment opportunities for all  qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.