Clarivate Hiring Associate Pharmacovigilance Specialist in Noida (Hybrid Mode)
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(Clarivate Hiring Associate Pharmacovigilance Specialist in Noida) |
Introduction
If you are looking for pharmacovigilance jobs in India, especially in ICSR processing and biomedical literature review, this is an excellent opportunity. Clarivate is hiring an Associate Pharmacovigilance Specialist in Noida, Uttar Pradesh (Hybrid work mode).
This role is ideal for freshers and early-career professionals with up to 2 years of experience in pharmacovigilance, drug safety, or biomedical literature screening. Candidates with a Master’s degree in Life Sciences or related fields can apply.
For aspirants targeting entry-level pharmacovigilance careers in India, this position provides structured training and exposure to global drug safety standards.
About The Company
Clarivate is a global leader in providing trusted insights and analytics to accelerate innovation. The company was founded in 2016 and is headquartered in London, United Kingdom.
Clarivate operates worldwide with approximately 12,000+ employees across multiple countries. It serves pharmaceutical companies, research institutions, universities, and government organizations by offering scientific data, intellectual property solutions, and life sciences insights.
The Life Sciences division of Clarivate plays a crucial role in biomedical literature monitoring, pharmacovigilance services, regulatory intelligence, and safety data analysis for global clients.
Job Overview Summary
The Associate Pharmacovigilance Specialist position in Noida focuses primarily on biomedical literature monitoring and Individual Case Safety Report (ICSR) identification.
The selected candidate will analyze scientific publications, identify adverse events, prepare safety narratives, and ensure compliance with global pharmacovigilance regulations. The role demands strong analytical skills and knowledge of medical terminology.
This is a hybrid role with fixed working hours and offers exposure to international drug safety processes.
Vacancy Details (Official Information)
Position: Associate Pharmacovigilance Specialist
Company: Clarivate
Location: Noida, Uttar Pradesh, India
Work Mode: Hybrid
Experience: Fresher / 0–2 Years
Industry: Pharmacovigilance / Drug Safety / Life Sciences
Posted On: 28 February 2026
Employment Type: Full-Time
Working Hours:
9:00 AM – 6:00 PM IST
OR
11:00 AM – 8:00 PM IST
Responsibility Explanation (In Simple Words)
The Associate Pharmacovigilance Specialist will perform the following core tasks:
• Review biomedical journals and research articles to identify adverse drug reactions
• Extract safety-relevant data for Individual Case Safety Reports (ICSRs)
• Write structured and concise safety narratives
• Monitor scientific literature as per regulatory requirements
• Assess drug labels and therapeutic area information
• Maintain compliance with pharmacovigilance SOPs
• Ensure documentation is audit-ready
• Work within safety databases and literature tracking systems
This role is critical in ensuring patient safety and regulatory compliance.
Eligibility Criteria (Official)
Master’s Degree in:
Pharmacy
Microbiology
Biotechnology
Biochemistry
Biophysics
Life Sciences
Biomedical Sciences
Experience:
Fresher OR up to 2 years in biomedical literature review or pharmacovigilance
Preferred:
Experience in pharmacovigilance literature screening
Skills Required (Expanded)
Candidates should possess:
• Strong knowledge of biomedical terminology
• Understanding of global pharmacovigilance regulations
• Analytical thinking and summarization ability
• Familiarity with literature databases like PubMed and Embase
• Strong written and verbal English communication skills
• Time management and adherence to SOPs
• Attention to detail in ICSR identification
Salary Estimate (Unique Explanation)
The estimated salary for an Associate Pharmacovigilance Specialist in Noida is:
₹3.5 LPA – ₹5.5 LPA (CTC)
Freshers may start closer to ₹3.5 LPA, while candidates with prior literature review or ICSR experience may negotiate towards ₹5.5 LPA.
Hybrid work flexibility and international exposure add additional career value beyond salary.
Interview Details (Official Process)
Application Mode: Online
Shortlisting: Based on academic qualification and PV exposure
Interview Rounds:
HR Screening
Technical Round (Pharmacovigilance & Literature Review)
Final Managerial Discussion
The selection process may vary depending on business needs.
Required Documents
Updated Resume with detailed academic background
Master’s Degree Certificate
Internship/Experience Letters (if any)
Government ID Proof
Academic Mark Sheets
Proof of literature review or PV training (if applicable)
Location
Job Location: Noida, Uttar Pradesh
Work Mode: Hybrid
Candidates may need to visit the office as per the hybrid policy.
Apply Method
Interested candidates can apply through:
Naukri Portal Link:
Official Clarivate Careers Link:
Apply early, as fresher PV roles receive high application volume.
FAQs Section
Q1. Can freshers apply for this pharmacovigilance job?
Yes, freshers with a Master’s degree in Life Sciences or related fields can apply.
Q2. Is prior ICSR experience mandatory?
No, but a biomedical literature review experience is preferred.
Q3. What is the work mode?
Hybrid mode in Noida.
Q4. What is the salary range?
₹3.5 – ₹5.5 LPA depending on experience.
Q5. What skills are most important?
Biomedical terminology knowledge, analytical skills, and safety narrative writing.
Final Conclusion
The Associate Pharmacovigilance Specialist role at Clarivate is an excellent entry point into the pharmacovigilance and drug safety industry.
With exposure to biomedical literature monitoring, ICSR processing, and global regulatory compliance, this position provides a strong foundation for long-term career growth in pharmacovigilance.
Candidates aiming for Drug Safety Associate, PV Specialist, or Global Safety roles should consider applying promptly.
Note: Pharma Duniya does not charge any money for job information.
Candidates are advised to verify details from the official company website.
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