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.