- Prioritize and complete the assigned trainings on time.
- Process Safety data according to applicable regulations, guidelines, Standard Operating Procedures (SOPs), and project requirements.
- Perform Pharmacovigilance activities per project requirements, including but not limited to:
- Collecting and tracking incoming Adverse Events (AE)/endpoint information.
- Determining the initial/update status of incoming events.
- Database entry.
- Coding AE and Products, writing narratives, literature-related activities.
- Assume other workflow responsibilities for the assigned project as directed by Operations team members or Manager.
- Ensure to meet the expected productivity and quality standards.
- Identify quality problems and bring them to the attention of a senior team member/mentor.
- Attend project team meetings and provide feedback to the operations manager on any challenges/issues or successes.
- Ensure 100% compliance towards all people practices and processes.
- Perform other duties as assigned.
Please email your updated CV to subudhi.bhanuja@iqvia.com
