Key Responsibilities:
As a Safety Associate at IQVIA, you will play a crucial role in pharmacovigilance and drug safety operations. Your primary responsibilities will include:
✔ Review and process safety data from various sources in compliance with regulatory standards.
✔ Perform ICSR (Individual Case Safety Report) case processing using Argus Safety Database.
✔ Conduct pharmacovigilance activities, including:
- Tracking Adverse Events (AEs) and endpoint information
- Determining initial/update status of incoming events
- Database entry, medical coding (MedDRA/WHO-DD), and narrative writing
- Managing literature-related safety reports
✔ Ensure 100% compliance with SOPs, global drug safety regulations, and project timelines.
✔ Maintain high quality, accuracy, and productivity in case processing.
✔ Collaborate with senior team members to resolve quality issues.
✔ Participate in team meetings and contribute to process improvements.
Must-Have Skills:
- 1-2 years of experience in Drug Safety, ICSR Case Processing, and Argus Database
- Strong knowledge of medical terminology and pharmacovigilance regulations
- Proficiency in Microsoft Office and web-based applications
- Attention to detail, ability to work in a team, and meet deadlines
Educational Qualifications:
- B.Pharm / M.Pharm / Pharm.D
About IQVIA
IQVIA (NYSE: IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. With over 82,000 employees worldwide, IQVIA helps biotech, pharmaceutical, and healthcare companies accelerate innovation and improve patient outcomes.
Why Join IQVIA?
✅ Global leader in healthcare intelligence & clinical research
✅ Learning & career growth opportunities
✅ Inclusive work culture with a focus on innovation
✅ Competitive salary and benefits
How to Apply
