IQVIA is a global leader in clinical research, healthcare intelligence, and life sciences analytics. With a mission to accelerate medical advancements, IQVIA provides data-driven insights 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
✔ Process and assess pharmacovigilance data from multiple sources.
✔ Enter and track Adverse Events (AEs) in databases.
✔ Ensure data accuracy and compliance with SOPs.
✔ Collaborate with project managers, medical teams, and clients.
✔ Support training and mentoring of new team members.
✔ Maintain 100% compliance with regulatory and company guidelines.
Essential Skills & Qualifications
✅ Education:
- High School Diploma (Required)
- Bachelor’s degree in Life Sciences/Pharmacy/Healthcare (Preferred)
✅ Experience:
- 1-3 years in pharmacovigilance/drug safety (Preferred)
- JLPT N3/NAT-Q3 certification is mandatory
✅ Technical Skills:
- Knowledge of medical terminology
- Proficiency in Microsoft Office & safety databases
- Strong verbal/written communication in English & Japanese
✅ Soft Skills:
- Attention to detail
- Time management & multitasking
- Problem-solving & teamwork
Benefits & Work Culture
💼 Job Type: Full-time
🌍 Industry: Pharmaceutical/Healthcare
🏢 Work Mode: On-site (Pune)
🔄 Shift Flexibility: Required
Why Join IQVIA?
✔ Global exposure in clinical research & pharmacovigilance
✔ Career growth opportunities
✔ Competitive salary & benefits
✔ Inclusive & innovative work culture
