Clarivate Hiring for Associate Pharmacovigilance Specialist
Position: Associate Pharmacovigilance Specialist
Company: Clarivate
Location: Noida & Bangalore (Hybrid)
Qualification: Master’s Degree in Life Sciences, Health, or Biomedical Sciences
Experience: Fresher – 2 Years
Work Mode: Hybrid
Job Type: Full-time
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About the Company
Clarivate is a global leader in analytics, research intelligence, and data-driven insights for healthcare and life sciences. The company empowers professionals across the world with accurate, evidence-based solutions for advancing scientific research, innovation, and patient safety. Clarivate Hiring for Associate Pharmacovigilance Specialist
As part of Clarivate’s commitment to medical excellence, the Pharmacovigilance (PV) team plays a vital role in supporting global clients by monitoring and analyzing biomedical literature to ensure drug safety and compliance with regulatory requirements. Clarivate Hiring for Associate Pharmacovigilance Specialist
About the Role
Clarivate is seeking dedicated and detail-oriented individuals for the role of Associate Pharmacovigilance Specialist in Noida and Bangalore.
This position offers a hybrid work model, providing a balance between remote flexibility and in-office collaboration. Clarivate Hiring for Associate Pharmacovigilance Specialist
The Associate PV Specialist will be responsible for monitoring biomedical literature, identifying adverse events, and supporting drug safety reporting for pharmaceutical clients.
This is an excellent opportunity for life sciences postgraduates and freshers who are passionate about pharmacovigilance, medical research, and regulatory affairs. Clarivate Hiring for Associate Pharmacovigilance Specialist
Key Responsibilities
As an Associate Pharmacovigilance Specialist at Clarivate, your primary duties will include: Clarivate Hiring for Associate Pharmacovigilance Specialist
- Conducting biomedical literature monitoring for adverse event (AE) detection and reporting.
- Assessing and summarizing scientific and medical case reports, journals, and publications.
- Applying knowledge of medical terminology, drugs, and therapeutic areas for accurate data classification.
- Performing indexing, abstracting, and annotation of literature records in compliance with pharmacovigilance standards.
- Supporting global safety teams by identifying relevant case reports for drug safety and risk management.
- Ensuring adherence to regulatory guidelines such as ICH, GVP, and MedDRA.
- Collaborating with cross-functional teams to meet timelines and quality standards.
Qualifications & Eligibility
Educational Requirement:
- Master’s Degree in Life Sciences, Health Sciences, or Biomedical Sciences
(Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.)
Experience:
- Freshers or candidates with up to 2 years of experience in pharmacovigilance, literature review, or biomedical research.
- Experience in drug safety or adverse event reporting is an added advantage.
Preferred Skills:
- Strong analytical and comprehension skills to summarize medical literature.
- Familiarity with pharmacovigilance databases and literature screening tools.
- Good understanding of medical terminology, therapeutic areas, and drug classifications.
- Excellent written and verbal communication skills.
- Scientific or medical writing background is desirable.
Preferred Additional Qualifications
- Certification from a professional medical writer’s association.
- Degree in Dentistry, Physiotherapy, or Nursing, especially with hospital-based experience.
- Hands-on experience with client-specific biomedical databases.
Work Schedule
- Days: Monday to Friday
- Timings: 12:00 PM – 9:00 PM (Hybrid Work Model)
Why Join Clarivate?
- Opportunity to work with a global leader in scientific research and data analytics.
- Exposure to international pharmacovigilance practices and compliance standards.
- A hybrid work environment that promotes flexibility and work-life balance.
- Supportive team culture focused on learning, innovation, and career growth.
- Equal opportunity employer committed to diversity, inclusion, and fair employment practices.
- Clarivate Hiring for Associate Pharmacovigilance Specialist
Equal Employment Opportunity
Clarivate is an equal opportunity employer. The company promotes a workplace free from discrimination based on race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability. Clarivate Hiring for Associate Pharmacovigilance Specialist
📅 Important Dates
- Posted On: October 27, 2025
- Application Deadline: November 7, 2025
📝 How to Apply
Interested and eligible candidates can apply through the official Clarivate career portal using the link below: Clarivate Hiring for Associate Pharmacovigilance Specialist
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