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Stem Content Analyst

Clarivate
Clarivate
3-5 years
Not Disclosed
Hyderabad, India
10 Feb. 18, 2026
Job Description
Job Type: Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

STEM Content Analyst – Regulatory Intelligence (Life Sciences)

Location: Hyderabad, India
Work Model: Hybrid (Monday–Friday)
Working Hours: 8:00–9:00 AM to 5:00–6:00 PM IST
Industry: Life Sciences & Healthcare – Regulatory Affairs
Job ID: JREQ134851
Posted Date: February 2, 2026

The Pharma Daily is hiring a STEM Content Analyst – Regulatory Intelligence to join a high-performing Life Sciences Regulatory Intelligence team. This role is ideal for regulatory affairs professionals with strong expertise in global pharmaceutical regulations, biologics, advanced therapies, and healthcare compliance frameworks.

The selected candidate will monitor global regulatory developments, interpret complex regulatory requirements, and deliver structured, high-quality regulatory intelligence content within an AI-enhanced editorial environment. This position plays a critical role in ensuring regulatory accuracy, content integrity, and operational efficiency across global markets.

Experience Required

Minimum 3–5 years of professional experience in regulatory affairs, regulatory intelligence, pharmaceutical development, quality compliance, or related life sciences roles.
Hands-on experience interpreting global health authority regulations and legislative updates.
Exposure to AI-assisted editorial workflows or validation of AI-generated regulatory content is preferred.

Educational Qualifications

Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Chemistry, Regulatory Affairs, or related discipline.
Advanced certifications in Regulatory Affairs or Quality Compliance are advantageous.

Core Skills and Competencies

Strong understanding of global regulatory frameworks including FDA, EMA, WHO, and national Ministries of Health.
Ability to interpret legislation, guidance documents, and regulatory updates across pharmaceuticals, biologics, advanced therapies, medical technologies, and digital health.
Knowledge of regulatory lifecycle management including submissions, approvals, and post-approval variations.
Strong analytical judgment and contextual interpretation skills.
Familiarity with AI/ML-enabled content production tools and digital transformation initiatives in regulatory affairs.
Excellent written communication skills with strong editorial precision and attention to detail.
Ability to collaborate effectively with global and cross-functional teams.
Fluency in English; additional languages are an advantage.

Key Responsibilities

Monitor global and regional regulatory updates from health authorities and international regulatory bodies.
Interpret and contextualize complex regulatory requirements impacting pharmaceutical and life sciences products.
Develop structured regulatory intelligence content for country modules and internal databases.
Analyze legislation, guidance documents, and consultation papers to assess impact on regulatory submissions and lifecycle management.
Collaborate within AI-enabled content production workflows, applying expert oversight for quality assurance and accuracy.
Coordinate with external consultants and local regulatory experts to validate country-specific regulatory information.
Communicate key regulatory insights to product, technology, and customer-facing teams.
Support cross-functional initiatives including AI workflow optimization, product enhancements, quality compliance improvements, and global content harmonization.

About the Team

The Regulatory Intelligence team operates within a global Regulatory Market Access framework, delivering trusted regulatory insights across the full lifecycle of pharmaceutical and life sciences products. The team collaborates with Product, Technology, Customer Care, and external experts to support compliance, strategic decision-making, and market access initiatives worldwide. Team members are distributed across multiple international locations, fostering a diverse and collaborative working environment.

Work Schedule

Full-time position – 40 hours per week.
Hybrid work model (Monday to Friday).
Based in Hyderabad, India.

Equal Employment Opportunity

The employer is committed to providing equal employment opportunities to all qualified candidates in hiring, compensation, promotion, training, and other employment-related practices in compliance with applicable laws and regulations.