Location– Pune
Job Overview:
Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process, which may include safety data collected from clinical trials and/or post marketing settings (i.e., unsolicited reports).
Summary of Responsibilities:
- Perform case intake and triage of the incoming safety information or reports from various sources either spontaneously or from a clinical trial.
- Assist with processing of the adverse events, including but not limited to:
- Data entry of safety data onto adverse event tracking systems.
- Write patient narratives and code adverse events accurately using MedDRA (for Marketed products, if applicable).
