About the job

We are a service provider company, leader in the Pharmaceutical and Medical Device sectors since 1998, with more than 1200 employees, 45+ nationalities and 28 subsidiaries all over the world (Europe, Asia and the Americas). Joining PQE means being a part of a multicultural and challenging company, with many local and international projects, and colleagues from all over the world.

Due to a constant growth, PQE is looking for Consultant/Senior Consultant- Pharmacovigilance Officers to join our PV Team who will be responsible for Pharmacovigilance related activities in India.

We are searching for a team of a PV officers.

𝑹𝑬𝑺𝑷𝑶𝑵𝑺𝑰𝑩𝑰𝑳𝑰𝑻𝑰𝑬𝑺 :

· Working knowledge of Pharmacovigilance-related areas (e.g. Data Management, Monitoring or equivalent professional background and experience).

· Good knowledge of ICH / Good Pharmacovigilance Practices (GVP).

· Good knowledge of medical/drug coding process (MedDRA and WHO drug dictionary).

· Basic knowledge of vaccine pharmacovigilance, as applicable.

· Basic knowledge of International clinical trial directive, as applicable – Proficient computer knowledge (Standard Microsoft Office applications).

· Working under supervision of the PV manager, project coordinator.

· Ability to perform Electronic reporting of ICSRs via email/CA database/gateway after corresponding training.

· Capability to work in an high level of accuracy in compliance with instructions and requirements.

𝑹𝑬𝑸𝑼𝑰𝑹𝑬𝑴𝑬𝑵𝑻𝑺 :

💼 𝐑𝐞𝐥𝐞𝐯𝐚𝐧𝐭 𝐄𝐱𝐩𝐞𝐫𝐢𝐞𝐧𝐜𝐞 in healthcare or pharmaceutical industry e.g: Laboratory Experience preferred.

💊 General knowledge of drug therapy, disease states, clinical research.

🎓 𝐃𝐞𝐠𝐫𝐞𝐞 (in life science or nursing/pharmacy qualification).

📚 𝐄𝐧𝐠𝐥𝐢𝐬𝐡 𝐟𝐥𝐮𝐞𝐧𝐭 (both oral and written)

⏳ Ability to work in due timelines.

✈️ Up to 10-15% travel, as needed, for project team meetings

📍 Available for 𝑷𝑨𝑵 𝑰𝑵𝑫𝑰𝑨 locations.

Location: PAN INDIA LOCATIONS (Ready to Travel as per business requirements) !

Apply through this Link