• 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