Global information and analytics company Clarivate has announced recruitment for the position of Associate STEM Content Analyst in Chennai, India. This opportunity is ideal for candidates with a background in Life Sciences, Pharmacy, Biotechnology, Chemistry, or Regulatory Affairs who have 1–2 years of pharmaceutical industry experience, particularly in CMC manufacturing or regulatory affairs.
The role offers exposure to global regulatory frameworks, structured content management, and AI-assisted workflows while working with international teams across France, Malaysia, India, Serbia, Spain, and the United States.
Job Details
- Position: Associate STEM Content Analyst
- Company: Clarivate
- Location: Chennai, Tamil Nadu, India
- Job Type: Full-Time
- Work Mode: Hybrid
- Department: Regulatory Market Access – CMC Team
- Experience Required: 1–2 Years
- Posted Date: 16 June 2026
Key Responsibilities
As an Associate STEM Content Analyst at Clarivate, you will:
- Maintain and update the global CMC regulatory database with accurate and standardized information.
- Monitor worldwide CMC regulatory updates, guidelines, and country-specific requirements.
- Analyze regulatory changes and convert them into structured content using defined methodologies.
- Document differences between local regulatory requirements and the Common Technical Document (CTD) framework.
- Collaborate with external consultants and subject matter experts to validate regulatory practices.
- Support product enhancements and content preparation activities.
- Provide regulatory expertise to internal stakeholders, including Product, Technology, and Customer Care teams.
- Assist in responding to customer queries under supervision.
- Apply editorial rules, taxonomies, and structured data standards consistently.
- Conduct quality checks and validation activities to maintain content governance standards.
- Participate in process improvement initiatives, automation projects, and data quality programs.
Educational Qualifications
Candidates should possess a Bachelor’s degree in any of the following disciplines:
- Pharmacy
- Life Sciences
- Biotechnology
- Chemistry
- Regulatory Affairs
- Other relevant science disciplines
Experience and Skills Required
Applicants should have:
- 1–2 years of pharmaceutical industry experience, preferably in CMC manufacturing or regulatory affairs.
- Understanding of global regulatory frameworks including FDA, EMA, and ICH guidelines.
- Familiarity with structured data environments and content management systems.
- Exposure to AI-assisted workflows and data validation processes.
- Excellent written communication and editorial skills.
- Strong analytical and problem-solving abilities.
- Ability to work in a collaborative international environment.
- Fluency in English.
Preferred Qualifications
Candidates with the following additional skills will have an advantage:
- Knowledge of ICH quality guidelines for small molecules and biologics.
- Exposure to regulatory submissions such as MAA, BLA, and ANDA.
- Understanding of regulatory intelligence and requirement comparison methodologies.
- Knowledge of an additional European language.
Why Join Clarivate?
Joining Clarivate as an Associate STEM Content Analyst provides:
- Opportunity to work on global CMC regulatory intelligence projects.
- Exposure to advanced content management and AI-assisted technologies.
- Collaboration with international teams and subject matter experts.
- Hybrid work flexibility.
- Career growth in pharmaceutical regulatory affairs and structured content analytics.
- Experience with global health authority requirements and regulatory data governance.
Work Schedule
- Work Mode: Hybrid
- Working Hours: Approximately 8:00–9:00 AM to 5:00–6:00 PM IST
How to Apply
