Associate Pharmacovigilance Specialist

Why This Role Matters

Pharmacovigilance specialists help ensure the safety of medicines by monitoring scientific literature and identifying potential adverse drug reactions. Their work supports regulatory compliance and helps pharmaceutical companies maintain safe and effective medications for patients worldwide.

Job Description

Clarivate is hiring an Associate Pharmacovigilance Specialist for its Life Sciences & Healthcare division in Noida, Uttar Pradesh. This role focuses on reviewing biomedical literature, identifying safety signals, and documenting adverse event information in compliance with pharmacovigilance regulations. It is an excellent opportunity for fresh graduates or early-career professionals interested in drug safety and pharmacovigilance.

Key Features of the Role

• Position: Associate Pharmacovigilance Specialist
• Company: Clarivate
• Location: Noida, Uttar Pradesh, India
• Industry: Life Sciences & Healthcare / Pharmacovigilance
• Employment Type: Full-Time
• Work Mode: Hybrid
• Experience Required: Fresher – 2 years

Responsibilities

• Review biomedical literature and internal safety alerts to identify potential adverse events
• Analyze and summarize biomedical case reports, research studies, and safety-related information
• Identify Individual Case Safety Reports (ICSRs) relevant to drug safety monitoring
• Prepare brief narratives summarizing safety findings from literature
• Assess safety information based on drug labeling and regulatory requirements
• Ensure timely and accurate completion of drug safety literature reviews
• Track safety assessments and actions using pharmacovigilance systems
• Follow standard operating procedures and regulatory compliance guidelines

Required Qualification

• Master’s Degree in Life Sciences, Health Sciences, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.)

Important Requirements

• 0–2 years of experience in biomedical literature review or pharmacovigilance
• Knowledge of biomedical terminology, drugs, and therapeutic areas
• Familiarity with biomedical literature databases
• Strong analytical and summarization skills
• Excellent written and verbal communication in English
• Ability to work in a fast-paced environment and adhere to SOPs

Work Schedule

• Hybrid work mode
• Monday to Friday
• 9:00 AM – 6:00 PM IST or 11:00 AM – 8:00 PM IST

What We Offer

• Hybrid working environment
• Exposure to global pharmacovigilance projects
• Personalized training and professional development opportunities
• Opportunity to work with international pharmaceutical clients

Experience and Skills

• Biomedical literature analysis
• Pharmacovigilance and drug safety monitoring
• Medical terminology and therapeutic area knowledge
• Data analysis and case report summarization
• Time management and attention to detail

Company Overview

Clarivate is a global information and analytics company that provides trusted insights and data-driven solutions for life sciences, healthcare, academia, and technology industries. The pharmacovigilance team at Clarivate supports global pharmaceutical companies by monitoring drug safety and ensuring compliance with international regulatory standards.

FAQs

1. What qualification is required for this role?
   Candidates must have a Master’s degree in Life Sciences or a related biomedical field.

2. Is experience required for this role?
   Freshers can apply, but candidates with up to 2 years of relevant experience are preferred.

3. Where is the job located?
   The role is based in Noida, Uttar Pradesh, India with a hybrid work mode.

4. What are the working hours?
   The team works Monday to Friday with shifts from 9 AM–6 PM or 11 AM–8 PM IST.

Application Tips

• Highlight your Master’s degree in Life Sciences or related field
• Mention knowledge of biomedical terminology and pharmacovigilance concepts
• Showcase experience in literature review or research analysis
• Emphasize analytical thinking and communication skills