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Associate Pharmacovigilance Specialist

Clarivate
Clarivate
0-2 years
Not Disclosed
Noida, India
10 Feb. 17, 2026
Job Description
Job Type: Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Pharmacovigilance Specialist 

Industry: Life Sciences & Healthcare
Employment Type: Hybrid
Job ID: JREQ134096
Posted Date: February 16, 2026

Job Overview

The Associate Pharmacovigilance Specialist is responsible for monitoring, analyzing, and reporting adverse events from biomedical literature, ensuring drug and patient safety in compliance with global pharmacovigilance regulations. The role requires expertise in medical terminology, therapeutic areas, and safety assessment processes.

This position is ideal for life sciences professionals seeking a dynamic environment in pharmacovigilance with exposure to global clients and cutting-edge safety evaluation practices.


Key Responsibilities

  • Review and critically analyze biomedical literature, published studies, and internal drug safety alerts to identify Individual Case Safety Reports (ICSRs) and other relevant safety information.

  • Prepare concise narratives summarizing ICSRs and potential safety concerns based on client-specific and regulatory requirements.

  • Apply knowledge of drug labels and therapeutic areas to assess safety signals accurately.

  • Perform timely and accurate safety reviews of literature batches according to client standards and SOPs.

  • Document all safety assessments and actions using drug safety systems to maintain an audit-ready reference history.

  • Collaborate with a global pharmacovigilance team to support multiple therapeutic areas.


Qualifications & Experience

  • Education: Master’s degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, or related field).

  • Experience: Fresher to 2 years of experience in biomedical literature review, adverse event reporting, or equivalent combination of education and relevant experience. Experience with information science plus at least 1 year in drug/patient safety is also acceptable.

  • Strong analytical skills to extract and summarize safety data from complex biomedical information.

  • Familiarity with biomedical terminology, drugs, therapeutic areas, and pharmacovigilance regulations.

  • Experience using commercial and client-specific biomedical literature databases.

Preferred Skills:

  • Excellent written and verbal English communication.

  • Effective time management and organizational skills.

  • High motivation and ability to thrive in a fast-paced environment.

  • Strong adherence to SOPs and corporate policies.


Work Environment

The position is hybrid, based in Noida or Bangalore, India, with work hours from 9:00 AM to 6:00 PM IST or 11:00 AM to 8:00 PM IST (Monday–Friday).

The pharmacovigilance team provides global clients with high-quality drug safety services across multiple therapeutic areas. The environment is collaborative, supportive, and offers continuous learning opportunities, including exposure to different pharmacovigilance processes and client engagement.


Why Join

  • Work in a global pharmacovigilance team supporting multiple therapeutic areas.

  • Gain exposure to international drug safety standards and regulatory practices.

  • Access to personalized training and career growth opportunities.

  • Hybrid working model with flexible hours.


Equal Opportunity Employer:
Our organization is committed to providing equal employment opportunities to all qualified individuals regarding hiring, compensation, promotion, training, and other employment terms. We strictly adhere to all local and international non-discrimination laws.


Apply Today:
Submit your application to be part of a growing global pharmacovigilance network and contribute to enhancing patient safety worldwide.