Looking for Drug Safety Associate jobs in India? Freyr Solutions is hiring Drug Safety Associates for its Global Regulatory Intelligence and Pharmacovigilance team. This is a remote pharmacovigilance job offering professionals the opportunity to work on global drug safety surveillance, regulatory intelligence, safety monitoring, signal detection, and safety data analysis.

If you have experience in pharmacovigilance, drug safety, regulatory intelligence, MedDRA coding, or safety surveillance, this opportunity provides exposure to international regulatory agencies, scientific literature monitoring, and emerging safety risk assessment.

Job Highlights

About Freyr Solutions

Freyr Solutions is a global regulatory solutions company providing end-to-end services in regulatory affairs, pharmacovigilance, medical writing, quality compliance, and life sciences consulting. The organization supports pharmaceutical, biotechnology, medical device, and consumer healthcare companies across multiple international markets.

Drug Safety Associate Job Description

As a Drug Safety Associate, you will support Global Regulatory Intelligence by monitoring worldwide health authority communications, regulatory updates, scientific literature, safety alerts, product recalls, and emerging pharmacovigilance information.

The role focuses on identifying potential safety signals, supporting risk assessment activities, maintaining pharmacovigilance knowledge repositories, and preparing safety intelligence reports for internal stakeholders.

Key Responsibilities

Safety Intelligence & Pharmacovigilance

• Monitor global regulatory authority websites for safety updates.
• Track safety alerts, recalls, adverse drug reactions, and label changes.
• Review scientific literature and medical publications.
• Conduct routine pharmacovigilance surveillance activities.
• Monitor Healthcare Professional Communications.
• Support signal evaluation and safety assessments.

Regulatory Intelligence

• Monitor international regulatory announcements.
• Track emerging safety risks across products.
• Review global pharmacovigilance communications.
• Analyze regulatory trends.

Data Analysis

• Analyze safety trends across therapeutic areas.
• Prepare safety intelligence summaries.
• Generate executive dashboards.
• Identify potential safety signals.
• Support safety data analysis using internal and external sources.

Knowledge Management

• Classify and organize pharmacovigilance information.
• Maintain safety knowledge repositories.
• Manage metadata and regulatory documentation.
• Support content categorization activities.

Required Qualifications

Candidates should possess one or more of the following qualifications:

• B.Pharm
• M.Pharm
• Pharm.D
• BSc Life Sciences
• MSc Life Sciences
• Biotechnology
• Clinical Research
• Other relevant Life Sciences degree

Required Skills

Freyr Solutions is looking for candidates with:

• Understanding of Pharmacovigilance principles
• Knowledge of the drug safety lifecycle
• Experience reviewing safety and regulatory documents
• Strong analytical and research skills
• Familiarity with MedDRA terminology
• Knowledge of global pharmacovigilance regulations (preferred)
• Excellent written and verbal English communication
• Stakeholder management skills
• Team collaboration
• Customer-focused mindset
• Problem-solving ability
• Attention to detail

Preferred Candidate Profile

Ideal candidates may have experience in:

• Pharmacovigilance
• Drug Safety
• Regulatory Intelligence
• Signal Detection
• Literature Surveillance
• Safety Database Operations
• Regulatory Affairs
• Medical Writing
• Safety Case Processing
• Risk Management

Why Join Freyr Solutions?

Employees working in Freyr’s pharmacovigilance teams gain exposure to:

• Global regulatory agencies
• International pharmacovigilance projects
• Remote work opportunities
• Cross-functional collaboration
• Career growth in drug safety
• Advanced regulatory intelligence practices
• International pharmaceutical clients

How to Apply

Application Link