In the high-stakes world of pharmaceutical safety, one role stands out as the ultimate “watchdog” for patient health — the Pharmacovigilance (PV) Specialist. If you have a passion for life sciences and a sharp eye for clinical data, there’s a golden opportunity waiting for you in Noida.
A leading global intelligence firm, Clarivate, is currently hiring for the position of Associate Pharmacovigilance Specialist (Job ID: JREQ134096). This hybrid role is ideal for Master’s degree holders who want to bridge the gap between medical literature and drug safety.
What is Pharmacovigilance? 🤔
Pharmacovigilance (PV) refers to the science and activities involved in the detection, assessment, understanding, and prevention of adverse effects or drug-related problems.
Even after a drug is approved and launched in the market, monitoring never stops. PV professionals review global safety data and report adverse drug reactions to regulatory authorities such as:
- Food and Drug Administration (FDA)
- European Medicines Agency (EMA)
They ensure medicines remain safe for public use throughout their lifecycle.
Job Overview: Associate Pharmacovigilance Specialist 📢
- Role: Associate Pharmacovigilance Specialist
- Location: Noida, India 📍
- Work Model: Hybrid (Office + Remote)
- Employment Type: Full-Time
- Experience: Freshers to 2 Years
- Requisition ID: JREQ134096
This is an excellent entry-level opportunity in the drug safety and biomedical literature review domain.
Who Should Apply? 🎓
1️⃣ Educational Qualifications
Candidates must hold a Master’s Degree in relevant life science disciplines such as:
- M.Pharm (Pharmacy)
- Microbiology
- Biochemistry
- Biotechnology
- Biophysics
- Biomedical Sciences
- Life Sciences
2️⃣ Experience Requirements
- ✅ Freshers with strong medical terminology knowledge are welcome.
- ✅ Up to 2 years of experience in biomedical literature review or adverse event reporting is an added advantage.
3️⃣ Core Competencies
- Strong analytical and critical reading skills
- Knowledge of drug classes and therapeutic areas
- Familiarity with biomedical databases like PubMed and Embase
- Attention to detail in safety data extraction
What Will Your Daily Routine Look Like? 📝
As an Associate PV Specialist, you act as a medical data investigator.
🔎 Literature Monitoring
Review large volumes of published medical journals and internal safety alerts to identify Individual Case Safety Reports (ICSRs).
✍️ Narrative Writing
Prepare concise case narratives summarizing:
- Patient information
- Suspected drug
- Adverse event
- Clinical outcome
⚖️ Risk-Benefit Assessment
Assess whether new safety data impacts the overall benefit-risk profile of the product.
📂 Audit Readiness
Maintain proper documentation in drug safety databases to ensure regulatory compliance during inspections.
Why Noida is a Great Hub for PV Careers 🏙️
Noida has emerged as a major hub for:
- Pharmaceutical KPO companies
- Clinical Research Organizations (CROs)
- Global regulatory support centers
The hybrid model helps professionals balance productivity with flexibility while staying connected to Delhi-NCR’s expanding pharma ecosystem.
Soft Skills That Make You Stand Out ✨
- Excellent written English (global reporting standards)
- Time management and deadline adherence
- High ethical standards and integrity
- Strong work motivation
How to Apply 📩
Interested candidates can apply directly through the official Clarivate career portal:
Pro Tips Before Applying:
- Highlight knowledge of GCP (Good Clinical Practice) and GVP (Good Pharmacovigilance Practices) in your CV.
- Mention database experience (PubMed, Embase).
- Be prepared for an analytical or case-based assessment round.
Final Thoughts 💡
Pharmacovigilance is one of the most stable and recession-resistant career paths in the pharmaceutical industry. As long as medicines are being developed, drug safety professionals will always be in demand.
For Master’s graduates in life sciences, this Associate role in Noida is a powerful gateway into:
- Global regulatory affairs
- Drug safety operations
- Clinical research careers
- Medical writing
If you’re aiming for a long-term corporate pharma career, this opportunity is worth applying for today.
