About The Role

Vizen Life Sciences is seeking a dedicated Pharmacovigilance Trainer with strong ICSR process knowledge, end-to-end PV expertise, and hands-on experience with safety databases like Argus and Clinovo.

Key Responsibilities

• Deliver client-specific training and internal SOP training to new joiners
• Serve as a Subject Matter Expert (SME) for ICSR case processing, providing mentorship and guidance.
• Monitor, assess, and enhance trainees' performance and quality of work.
• Work on diverse post-marketing case types, ensuring compliance with GVP guidelines and regulatory requirements.
• Develop and conduct impactful presentations and training sessions to improve team knowledge and efficiency.
  
  

Must-Have Skills

• Strong knowledge of ICSR processes and GVP modules.
• Hands-on experience with safety databases like Clinovo and Argus.
• Excellent presentation, communication, and interpersonal skills.
• Proven experience as a trainer and SME in pharmacovigilance.
  
  

Qualifications

• Bpharm ,Pharm.D or M.Pharmacy.
  
  

Experience Required

• 4–8 years of overall pharmacovigilance experience in post-marketing, with exposure to various therapeutic areas, particularly pharmaceutical drugs. This includes at least 1–3 years of experience as a trainer or Subject Matter Expert.