Freyr Hiring Associate / Senior Associate - PV Regulatory Intelligence
Are you seeking Freyr Careers Remote or Pharmacovigilance Intelligence Analyst Jobs in India? Global regulatory solutions provider Freyr is hiring experienced drug safety professionals for the position of Associate / Senior Associate – Pharmacovigilance Global Regulatory Intelligence.
This remote safety intelligence monitoring vacancy is ideal for pharmacy (B.Pharm/M.Pharm) or engineering (B.E./B.Tech) graduates with 4 to 9 years of experience auditing global health authority updates, tracking safety signal registries, and reviewing scientific literature. Selected candidates will analyze safety trends and compile database records. To write a resume detailing your signal evaluations, literature searches, or metadata tracking, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | Freyr Solutions (Freyr Software Services Pvt Ltd) |
| Position | Associate / Senior Associate – Pharmacovigilance Global Regulatory Intelligence |
| Job Location | Remote (Hiring Office: Hyderabad, India) |
| Work Mode | Work from Home / Remote |
| Employment Type | Full-Time |
| Experience Required | 4–9 Years (Core Pharmacovigilance and Safety Analysis) |
| Qualifications | B.Pharm, M.Pharm, B.E./B.Tech, B.Sc, M.Sc in Life Sciences |
| Expected CTC | ₹4,00,000 – ₹9,00,000 per annum (Approx.) |
💼 Key Responsibilities
- Health Authority Monitoring: Audit global regulatory agency portals for safety warnings, label updates, and guidelines changes.
- Safety Alerts Review: Track safety alerts, drug recalls, risk minimization communications, and patient safety notifications.
- Literature Surveillance: Conduct systematic database review of scientific journals and medical publications for adverse drug reactions (ADRs).
- Signal Identification: Monitor and flag safety signals, assessing potential product safety trends across therapeutic areas.
- Dashboard Preparation: Draft intelligence reports and maintain safety metrics dashboards for pharmaceutical sponsors.
- Metadata Classification: Categorize and index regulatory intelligence records inside the safety information database.
To learn how remote pharmacovigilance intelligence and drug safety salaries compare to conventional data programmer and clinical trial coordinator structures, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- Education: Bachelor's or Master’s degree in Pharmacy, Life Sciences, or Engineering (B.Pharm or B.E./B.Tech preferred).
- PV Experience: 4 to 9 years of active experience in drug safety surveillance, signal detection, or regulatory affairs.
- Analytical Capability: Excellent research capabilities to analyze complex medical texts and abstract key safety findings.
- Regulatory Knowledge: Deep understanding of global health authority guidelines (such as FDA, EMA, MHRA, and CDSCO).
- MedDRA Expertise: Strong familiarity with MedDRA terminology coding and medical terminology structures.
For pharmacy graduates evaluating safety intelligence pathways compared to conventional laboratory quality control or direct dispensing chemist careers, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join Freyr?
- Work from the comfort of your home with a remote job setup supporting global biotech sponsors.
- Develop domain expertise in global regulatory intelligence frameworks and safety signals database tracking.
- Collaborative remote team structure with access to international projects.
- Stable full-time career path with competitive compensation structures.
To review your basic knowledge of clinical databases, safety protocols, and GCP guidelines before your screening calls, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Regulatory Intelligence vs Healthcare IT
PV Intelligence Associates audit health authority sites, track safety alerts, and manage compliance metadata databases, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Freyr Candidates
- Highlight Signal Tracking: Clearly detail experience with safety signal registries, literature reviews, or health authority trackers.
- Specify Agency Portals: Name the regulatory portals you have monitored (e.g. FDA, EMA, PMDA, MHRA).
- Show Remote Experience: If you have worked remotely before, mention your database access and digital team collaboration tools.
💬 Freyr PV Global Regulatory Intelligence Interview Questions
- Q1. What is the role of Global Regulatory Intelligence in pharmacovigilance?
Answer Guidance: Global Regulatory Intelligence is responsible for continuously monitoring, analyzing, and reporting changes in safety guidelines, label requirements, and hazard warnings issued by global health authorities to ensure sponsor compliance. - Q2. How do you assess a safety alert published on a foreign health authority website?
Answer Guidance: I log the alert source, identify the active drug substance, evaluate if the warning affects the sponsor's product range, verify if local labels cover the risk, and notify safety leads for further action. - Q3. Explain how literature review supports pharmacovigilance surveillance.
Answer Guidance: Literature review helps identify case reports of adverse events not reported through spontaneous channels, assists in signal detection for rare safety issues, and supplies peer-reviewed safety data for aggregate reporting.
🚀 How to Apply?
Interested and eligible candidates can submit their applications directly via Freyr's official Naukri careers listing. Click the button below to apply:
Apply Online – Freyr Naukri Listing❓ Frequently Asked Questions
Q. Is this Freyr regulatory intelligence role fully remote?
Yes, this is a full-time, Work from Home (Remote) position with the hiring office based in Hyderabad, India.
Q. Which degrees are preferred by the recruiters for this role?
Recruiters prefer candidates holding B.Pharm (Pharmacy) or B.E./B.Tech (Engineering/IT) qualifications.
Q. What is the required experience for senior associate roles?
Freyr requires 4 to 9 years of active experience in pharmacovigilance operations and safety intelligence systems.
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