- Case management of post marketing ICSRs (e.g., consumer, doctor, literature, , regulatory)
- Case management of clinical trial (Phase II , III)
- Understanding of 15 days and 90 days reporting of all cases.
- Hands on experience on any one of the safety database (Argus, Aris G, AB cube, Veeva)
- Understanding of serious, non-serious case and SUSAR
- Minimum 1-2 years of MedDRA coding and narrative writing experience.
- Minimum 1-2 years’ experience in data entry, triaging of cases, follow-up of case request