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Japanese Pharmacovigilance Openings in IQVIA

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IQVIAย is aย global leaderย inย clinical research, healthcare intelligence, and life sciences analytics. With a mission to accelerate medical advancements, IQVIA providesย data-driven insightsย to improve patient outcomes worldwide.

Detailed Job Description

Job Overview

The Operations Specialist 1 – Japanese Linguist will review and process safety data related to pharmacovigilance, ensuring compliance with regulatory standards (SOPs, global guidelines). The role involves handling Adverse Event (AE) reports, medical data entry, and liaising with healthcare professionals.

Key Responsibilities

โœ” Process and assess pharmacovigilance data from multiple sources.
โœ” Enter and track Adverse Events (AEs) in databases.
โœ” Ensure data accuracy and compliance with SOPs.
โœ” Collaborate with project managers, medical teams, and clients.
โœ” Support training and mentoring of new team members.
โœ” Maintain 100% compliance with regulatory and company guidelines.

Essential Skills & Qualifications

โœ… Education:

  • High School Diplomaย (Required)
  • Bachelorโ€™s degree in Life Sciences/Pharmacy/Healthcareย (Preferred)

โœ… Experience:

  • 1-3 yearsย inย pharmacovigilance/drug safetyย (Preferred)
  • JLPT N3/NAT-Q3 certification is mandatory

โœ… Technical Skills:

  • Knowledge ofย medical terminology
  • Proficiency inย Microsoft Office & safety databases
  • Strongย verbal/written communicationย inย English & Japanese

โœ… Soft Skills:

  • Attention to detail
  • Time management & multitasking
  • Problem-solving & teamwork

Benefits & Work Culture

๐Ÿ’ผ Job Type: Full-time
๐ŸŒ Industry: Pharmaceutical/Healthcare
๐Ÿข Work Mode: On-site (Pune)
๐Ÿ”„ Shift Flexibility: Required

Why Join IQVIA?

โœ” Global exposure in clinical research & pharmacovigilance
โœ” Career growth opportunities
โœ” Competitive salary & benefits
โœ” Inclusive & innovative work culture


How to Apply

Application Link

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