IQVIA Hiring Pharmacovigilance Safety Associate – Japanese Linguist Pune

IQVIA Hiring Pharmacovigilance Safety Associate – Japanese Linguist in Pune

Are you proficient in Japanese and have a background in life sciences? IQVIA is looking for a Pharmacovigilance Safety Associate – Japanese Linguist to join our team in Pune. This full-time role offers a great opportunity to advance your career in pharmacovigilance.

About the Job

Position: Pharmacovigilance Safety Associate – Japanese Linguist
Location: Pune, India
Employment Type: Full-Time

About IQVIA

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We push the boundaries of human science and data science to make a significant impact, helping our customers create a healthier world.

Job Description

As a Pharmacovigilance Safety Associate, you will review, assess, and process safety data and information across various service lines. You will distribute reports and data to both internal and external third parties following applicable regulations, SOPs, and internal guidelines under the guidance of senior operation team members.

Key Responsibilities:

• Case processing – cases in Japanese Language
• To Prioritize and complete the assigned trainings on time.
• Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.
• To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information
• determining initial/update status of incoming events
• database entry
• coding AE and Products, writing narratives, Literature related activities as per internal/ project  timelines.
• Ensure to meet quality standards per project requirements.
• Ensure to meet productivity and delivery standards per project requirements.
• To ensure compliance to all project related processes and activities.
• Creating, maintaining and tracking cases as applicable to the project plan.
• Identify quality problems, if any, and bring them to the attention of a senior team member.
• To demonstrate problem solving capabilities. To mentor new teams members, if assigned by the Manager.
• Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.
• 100% compliance towards all people practices and processes
• Perform other duties as assigned.

Qualifications

• Education: Bachelor’s degree in a scientific or healthcare discipline, or allied life sciences.
• Certification: JLPT N3/NAT certification.
• Experience: 1-1.5 years of relevant experience in pharmacovigilance.
• Skills:
  • Proficiency in medical terminology and safety databases.
  • Knowledge of global, regional, and local clinical research regulatory requirements.
  • Strong organizational, time management, and communication skills.
  • Self-motivated, flexible, and able to work independently as well as in a team.
  • Ability to multitask and manage competing priorities.

Why Join IQVIA?

Joining IQVIA means being part of a company that values innovation, collaboration, and professional growth. Our team members are passionate about their work, and we provide a dynamic work environment where you can learn, grow, and make a significant impact.

How to Apply

If you meet the qualifications and are excited about this opportunity, apply now to join IQVIA’s dynamic team in Pune. Submit your application through the IQVIA Direct Referral.

Tagged as: Global Pharma Jobs, Pharmaceutical Careers, Pharmaceutical Jobs