Job Description Pharmacovigilance (PV) Associate

We are expanding our Pharmacovigilance (PV) team across India, Singapore, and Japan, and are inviting motivated fresh graduates to join us. This is a unique prospect to begin a career in drug safety and regulatory operations while gaining international exposure and structured training.

Role Overview

As a PV Associate, you will undergo comprehensive training to support global pharmacovigilance activities. Your responsibilities will include case processing, literature review, and preparation of safety reports. You will collaborate with crossborder teams and contribute to projects that safeguard patient health and ensure compliance with international regulatory standards.

Requirements
Fresh graduates from Life Sciences (B.Pharm, M.Pharm, or related disciplines preferred).
Japanese language proficiency: JLPT N2 or above (read, write, speak).
Robust communication skills in English.




Eagerness to learn and grow in PV operations.

Benefits
Accommodation and food support during training and assignments.
Opportunities for business trips to Japan and Singapore to participate in client meetings and training programs.
Future work opportunities in Japan with visa sponsorship.
Exposure to international projects, regulatory environments, and growth opportunities in a global CRO setting.

This role is ideal for freshers who are passionate about healthcare, regulatory science, and international collaboration. By joining our team, you will gain handson experience, structured training, and the chance to build a longterm career in pharmacovigilance with opportunities to work abroad.(Singapore or Japan)

📌 Freshers Japanese Nellore (India)
🏢 SHIGOTO CONSULTANCY SERVICES
📍 India