Clarivate Hiring STEM Content Analyst | Pharma Professionals Apply Now
Are you searching for a Regulatory Affairs Job with a global leader in life sciences and healthcare intelligence? Clarivate Careers has announced an exciting opportunity for the position of STEM Content Analyst in Tamil Nadu, India. This Regulatory Affairs Job is ideal for professionals with experience in CMC regulatory affairs, regulatory intelligence, pharmaceutical development, and quality compliance who want to contribute to global regulatory content and AI-enabled workflows within Clarivate Careers.
- Job Title: STEM Content Analyst
- Location: Tamil Nādu, India
- Remote: Hybrid
- Job ID: JREQ135815
About the Company
Clarivate is a global leader in providing trusted insights and analytics to accelerate the pace of innovation. Through curated content, technology solutions, and expert intelligence, Clarivate supports organizations across healthcare, life sciences, academia, government, and intellectual property sectors. The company is committed to improving innovation through high-quality content, regulatory intelligence, and advanced technologies.
Job Description
Clarivate is hiring a STEM Content Analyst for its Regulatory Market Access team. The selected candidate will monitor and analyze global and regional CMC regulatory developments, transform regulatory updates into structured intelligence, collaborate with AI-enabled content workflows, and contribute to regulatory content standardization and quality initiatives.
Key Responsibilities
- Monitor global CMC regulatory guidelines, standards, and country-specific requirements.
- Review and interpret regulatory updates and assess their impact.
- Convert regulatory changes into structured regulatory intelligence content.
- Analyze CMC requirements within the CTD framework and identify regional differences.
- Evaluate regulatory updates affecting manufacturing, submissions, and product lifecycle management.
- Work with AI-powered content tools to improve data quality and efficiency.
- Maintain accurate, consistent, and traceable regulatory database content.
- Collaborate with consultants and regulatory experts to validate local requirements.
- Perform quality checks (QC) to ensure compliance with editorial and data standards.
- Share important regulatory insights with internal teams and stakeholders.
- Support workflow improvements, product enhancements, and data quality initiatives.
- Identify content gaps, risks, and inconsistencies and implement corrective actions.
Qualifications
Required Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Chemistry, Regulatory Affairs, or a related field.
- 3–5 years of experience in CMC regulatory affairs, regulatory intelligence, pharmaceutical development, or quality/manufacturing compliance.
- Strong knowledge of CMC requirements, CTD Module 3, and global regulatory frameworks (FDA, EMA, ICH, LATAM, APAC).
- Ability to interpret and analyze complex regulatory requirements independently.
- Experience handling evolving regulatory scenarios and making informed decisions.
- Background in content strategy, standardization, or data model enhancement.
- Experience reviewing regulatory guidelines, quality standards, and CMC regulatory updates.
- Familiarity with content management systems, regulatory databases, and structured data environments.
- Experience working with AI-assisted content workflows and validating AI-generated content.
- Excellent written communication and attention to detail.
- Ability to simplify complex regulatory information into clear, structured content.
- Strong collaboration skills for working with global and cross-functional teams.
- Fluency in English.
Preferred Qualifications
- Experience developing CMC regulatory intelligence or structured regulatory content.
- Knowledge of regulatory lifecycle management, submissions, approvals, and post-approval changes.
- Experience working with external consultants and local regulatory experts.
- Understanding of regulatory intelligence methodologies, trend analysis, and requirement comparison.
- Familiarity with quality management systems, data governance, and content standardization.
- Exposure to AI/ML-driven content production, automation, or digital transformation projects in regulatory affairs.
