06 Aug
|
Syneos Health
|
Hyderabad
06 Aug
Syneos Health
Hyderabad
Roles and Responsibilities :
- Process case reports of adverse events (AEs) and serious adverse events (SAEs) from clinical trials, literature, and other sources using Argus Safety software.
- Conduct thorough reviews of AE/SAE reports to identify potential signals and trends, ensuring compliance with regulatory requirements.
- Collaborate with cross-functional teams to resolve issues related to case processing, including data discrepancies and queries.
- Develop and maintain documentation for pharmacovigilance activities, such as protocols, procedures, and reports.
Job Requirements :
- 2-7 years' experience in pharmacovigilance or a related field (e.g., clinical trials).
- Robust understanding of Argus Safety software and its applications in drug safety surveillance.
- Experience working with MedDRA coding system for reporting adverse events.
- Bachelor's degree in Life Sciences or a related field; Master's degree preferred.
📌 Safety Specialist I/ II (Hyderabad)
🏢 Syneos Health
📍 Hyderabad