Clarivate Opens Regulatory Affairs Job for Pharmacy Professionals | Associate STEM Content Analyst Role
Looking for a rewarding Regulatory Affairs Job with a global leader? Clarivate Careers brings an exciting opportunity for an Associate STEM Content Analyst in Tamil Nadu, India. This hybrid position is ideal for Pharmacy graduates with 1–2 years of pharmaceutical industry experience. If you’re looking to build a successful career in CMC, global regulatory compliance, and structured content management, this Regulatory Affairs Job through Clarivate Careers could be the perfect opportunity.
- Job Title: Associate STEM Content Analyst
- Location: Tamil Nādu, India
- Remote: Hybrid
- Job ID: JREQ135817
About the Company
Clarivate is a global leader in providing trusted intelligence, technology, and expert solutions across life sciences, healthcare, academia, and intellectual property. The Regulatory Market Access team supports pharmaceutical companies by curating worldwide CMC regulatory content, monitoring global regulations, and delivering structured regulatory intelligence that helps improve innovation and compliance.
Job Description
Clarivate is looking for an Associate STEM Content Analyst to support its Regulatory Market Access team. The role focuses on maintaining and curating global CMC regulatory content, monitoring worldwide regulatory updates, supporting structured content creation, and collaborating with international experts to ensure regulatory accuracy and consistency
Key Responsibilities
- Maintain and update the global CMC regulatory database with accurate and reliable information.
- Monitor global CMC regulatory updates, new guidelines, and country-specific requirements.
- Analyze regulatory changes and convert them into standardized content.
- Document differences between local regulatory requirements and the CTD framework.
- Collaborate with regulatory experts to validate content and local practices.
- Support product updates and regulatory content enhancements.
- Provide regulatory support to Product, Tech, and Customer Care teams.
- Assist in responding to customer regulatory queries accurately.
- Follow editorial standards, workflows, and data management guidelines.
- Perform quality checks (QC) to ensure content accuracy and compliance.
- Contribute to process improvements, automation, and data quality initiatives.
Qualification
Required Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Chemistry, Regulatory Affairs, or a related field.
- 1–2 years of experience in the pharmaceutical industry, preferably in CMC manufacturing or CMC Regulatory Affairs.
- Basic knowledge of CMC requirements and global regulatory guidelines (FDA, EMA, ICH).
- Familiarity with content management systems and structured data environments.
- Exposure to AI-assisted workflows, data validation, or AI-generated content review.
- Excellent written communication skills with strong attention to detail.
- Ability to analyze regulatory information and create structured, standardized content.
- Ability to follow editorial standards, templates, and defined methodologies.
- Strong collaboration, problem-solving, and decision-making skills.
- Ability to work effectively in an international, remote team environment.
- Proactive mindset with excellent teamwork and communication skills.
- Fluent in English.
Preferred Qualifications
- Knowledge of ICH quality guidelines for small molecules and/or biologics.
- Experience with regulatory submissions such as MAA, BLA, or ANDA.
- Understanding of regulatory intelligence concepts and local regulatory practices.
- Knowledge of an additional European language is an advantage.
