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.
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