Are you an experienced pharmacovigilance professional looking for a remote opportunity in global regulatory intelligence? Freyr is hiring Associate and Senior Associate โ Pharmacovigilance Global Regulatory Intelligence professionals with 4โ9 years of experience. This role offers an exciting opportunity to work on global drug safety surveillance, regulatory intelligence, safety signal monitoring, MedDRA coding support, and health authority updates while collaborating with international stakeholders.
If you have expertise in pharmacovigilance, regulatory intelligence, drug safety, MedDRA, safety signal detection, and global regulatory compliance, this role could be your next career move.
Job Overview
| Details | Information |
|---|---|
| Company | Freyr |
| Position | Associate / Senior Associate โ Pharmacovigilance Global Regulatory Intelligence |
| Job Type | Full-Time |
| Experience | 4โ9 Years |
| Qualification | B.Pharm, B.E./B.Tech (Preferred) |
| Location | Remote (Hiring Office: Hyderabad) |
| Salary | โน4โ9 LPA (Approx.) |
| Industry | Pharmaceutical & Life Sciences |
Key Responsibilities
The selected candidate will be responsible for:
- Monitor global health authority websites for pharmacovigilance and regulatory updates.
- Review safety alerts, recalls, label changes, and risk minimization communications.
- Conduct surveillance of adverse drug reactions (ADR) and safety-related information.
- Review scientific literature, medical journals, conference proceedings, and public safety databases.
- Monitor healthcare professional letters and regulatory communications.
- Identify emerging safety risks and potential safety signals.
- Analyze safety trends across products, therapeutic areas, and global markets.
- Prepare regulatory intelligence reports and executive safety dashboards.
- Support signal evaluation and safety assessments.
- Maintain pharmacovigilance knowledge repositories and metadata.
- Classify and organize regulatory intelligence content.
- Collaborate with cross-functional teams supporting global pharmacovigilance activities.
Required Qualifications
Candidates should possess:
- B.Pharm or B.E./B.Tech degree.
- 4โ9 years of pharmacovigilance experience.
- Strong understanding of the pharmacovigilance lifecycle.
- Experience reviewing regulatory and safety-related documents.
- Familiarity with MedDRA terminology.
- Knowledge of global regulatory guidelines.
- Excellent analytical and research skills.
- Strong written and verbal English communication.
- Ability to work independently in a remote environment.
- Stakeholder management and teamwork skills.
Preferred Skills
Freyr is looking for professionals with experience in:
- Pharmacovigilance
- Global Regulatory Intelligence
- Drug Safety
- Regulatory Affairs
- MedDRA
- Safety Signal Detection
- Signal Evaluation
- Regulatory Surveillance
- Competitive Intelligence
- Market Intelligence
- Scientific Literature Review
- Health Authority Monitoring
- Risk Management
- Metadata Management
- Safety Reporting
Why Join Freyr?
Working at Freyr offers professionals the opportunity to:
- Work remotely with global pharmaceutical clients.
- Gain exposure to international pharmacovigilance regulations.
- Build expertise in regulatory intelligence and safety surveillance.
- Work on global health authority updates and safety signal detection.
- Collaborate with experienced drug safety professionals.
- Develop career growth in regulatory affairs and pharmacovigilance.
Salary
Based on the job posting and market standards, the expected salary is:
โน4,00,000 โ โน9,00,000 per annum (CTC)
Actual compensation may vary depending on experience, skills, and interview performance.
How to Apply
