As an Associate or Senior Associate- Pharmacovigilance Global Regulatory Intelligence, you would support safety intelligence and surveillance activities by monitoring public-domain sources, health authority communications, scientific literature, regulatory updates, and safety-related information to identify emerging risks, safety signals, and regulatory trends.

Key Responsibilities

Safety Intelligence & Monitoring
Monitor global health authority websites, regulatory agencies, and public databases for safety-related updates.
Track adverse drug reaction communications, recalls, label changes, safety alerts, and risk minimization measures.
Review scientific literature, conference proceedings, and medical publications for product-specific safety information.
Conduct routine surveillance of public-domain safety information.
Surveillance of Health care skilled letters, signal evaluation and assessments.

Data Analysis & Reporting
Analyze safety trends and emerging risks across products, therapeutic areas, and markets.




Prepare safety intelligence summaries and executive dashboards.
Identify potential safety signals from publicly available information.
Support trend analysis using internal and external datasets.

Knowledge Management
Classify and tag safety-related content.
Maintain pharmacovigilance knowledge repositories.
Support metadata management and content categorization.

Required Skills
Understanding of pharmacovigilance concepts and safety lifecycle.
Experience reviewing regulatory and safety-related content.
Robust analytical and research skills.
Familiarity with MedDRA and safety terminology.
Familiarity with global regulations in the pharmaceutical and/ or medical device industry is an added advantage
Ability to coordinate with stakeholders from multiple functions
Valuable English communication and interpersonal skills
A customer-first attitude
Problem-solving aptitude
Ability to work well with a team

📌 Pharmacovigilance Global Regulatory Intelligence Telangana
🏢 Freyr
📍 Telangana