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Associate Pharmacovigilance Specialist-7

0-1 years
upto 5 LPA
10 Nov. 18, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. 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

Associate Pharmacovigilance Specialist – Literature Screening

Location: Noida, Uttar Pradesh, India
Industry: Life Sciences & Healthcare
Work Mode: Hybrid
Job ID: JREQ134249
Posted On: November 17, 2025
Experience Required: Fresher (0-1 years)

Role Overview

This entry-level role is designed for graduates looking to begin their career in pharmacovigilance with a focus on literature screening and safety data evaluation. The position involves reviewing scientific publications, extracting key safety information, and supporting the identification of potential adverse events in alignment with global drug safety standards.

Key Responsibilities

  • Review scientific and medical literature under supervision to identify reports of adverse events, safety risks, or potential signals requiring further evaluation.

  • Extract relevant safety information from literature sources with accuracy and ensure completeness of all data captured for case processing and follow-up.

  • Enter validated safety data into pharmacovigilance databases or internal tracking systems while maintaining structured and compliant documentation.

  • Stay informed about current pharmacovigilance regulations, global safety guidelines, and evolving best practices to ensure compliant and high-quality literature screening activities.

Minimum Qualifications

  • Bachelor’s degree in Pharmacy, Life Sciences, Nursing, or a related discipline.

  • Freshers (0-1 years) with strong interest in pharmacovigilance are encouraged to apply.

About the Role Category

Pharmacovigilance literature screening plays a critical role in global drug safety. It involves systematically reviewing peer-reviewed journals, clinical research articles, and scientific publications to identify adverse drug reactions and emerging safety signals. Professionals in this domain support regulatory compliance by ensuring timely detection and reporting of safety-related information.

Equal Opportunity Commitment

Clarivate is committed to fostering an inclusive work environment. All qualified individuals will receive equal consideration in recruitment, compensation, career advancement, and training. The organization adheres to all applicable laws and regulations regarding non-discrimination across all operational locations.