STEM Content Analyst
Clarivate
full-time
Posted on:
Location Type: Hybrid
Location: Hyderabad • India
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About the 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
Requirements
- 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)
- 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
Benefits
- Hybrid work mode (Monday to Friday)
- Equal employment opportunities for all qualified persons
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
regulatory affairsregulatory intelligencepharmaceutical developmentquality compliancelegislation analysisguidance interpretationregulatory updates assessmentAI-assisted workflowsdata analysiscontextual judgment
Soft Skills
written communicationattention to detaileditorial precisioncollaborationcross-functional teamworkanalytical skillsorganizational skillscommunication skillsproblem-solvingadaptability
Certifications
Bachelor’s degree in Life SciencesBachelor’s degree in PharmacyBachelor’s degree in BiotechnologyBachelor’s degree in ChemistryBachelor’s degree in Regulatory Affairs