Pharmacovigilance - Global Regulatory Intelligence

Freyr Hiring: Associate / Senior Associate – Pharmacovigilance (Global Regulatory Intelligence)

Freyr is hiring Associate / Senior Associate – Pharmacovigilance (Global Regulatory Intelligence) professionals to support global drug safety surveillance, regulatory intelligence, and safety monitoring activities. This is an excellent opportunity for experienced Pharmacovigilance professionals looking to work in a remote role with exposure to global regulatory requirements and safety intelligence.

Position

Associate / Senior Associate – Pharmacovigilance (Global Regulatory Intelligence)

Company

Freyr

Job Location

Remote (Hiring office located in Hyderabad)

Openings

5 Positions

Experience Required

4–9 Years

Salary Package

₹4–9 LPA

Key Responsibilities

Safety Intelligence & Monitoring

• Monitor global health authority websites, regulatory agencies, and public databases for safety-related updates.
• Track adverse drug reaction (ADR) communications, product 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 publicly available drug safety information.
• Monitor Healthcare Professional (HCP) letters, signal evaluations, and safety assessments.

Data Analysis & Reporting

• Analyze emerging safety trends and product risks across therapeutic areas and global markets.
• Prepare safety intelligence summaries, reports, and executive dashboards.
• Identify potential safety signals using public-domain information.
• Support trend analysis using internal and external safety datasets.

Knowledge Management

• Classify and organize safety-related information.
• Maintain pharmacovigilance knowledge repositories.
• Support metadata management and content categorization.

Education

• B.Pharm
• B.E./B.Tech (Any Specialization)

Required Skills

• Good understanding of Pharmacovigilance concepts and the drug safety lifecycle.
• Experience reviewing regulatory and safety-related information.
• Knowledge of Regulatory Intelligence and global safety monitoring.
• Familiarity with MedDRA and pharmacovigilance terminology.
• Understanding of global pharmaceutical and medical device regulations is an added advantage.
• Strong analytical, research, and problem-solving skills.
• Excellent written and verbal communication skills.
• Ability to collaborate with cross-functional teams and global stakeholders.
• Customer-focused mindset with strong interpersonal skills.

Preferred Skills

• Pharmacovigilance
• Regulatory Intelligence
• Regulatory Affairs
• Market Intelligence
• Competitive Intelligence
• Safety Surveillance
• Signal Detection
• Drug Safety

Why Join Freyr?

• Remote work opportunity.
• Exposure to global Pharmacovigilance and Regulatory Intelligence projects.
• Work with international pharmaceutical and medical device clients.
• Opportunity to build expertise in global drug safety and regulatory compliance.
• Collaborative work environment with career growth opportunities.

About the Company

Freyr is a global life sciences solutions provider offering Regulatory Affairs, Pharmacovigilance, Medical Writing, Clinical Research, and Market Intelligence services to pharmaceutical, biotechnology, medical device, nutraceutical, and consumer healthcare companies worldwide.

How to Apply

Interested candidates can apply through the official Freyr Careers portal or the job listing platform by submitting their updated resume.