Mgr Pharmacovigilance

About the role

Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together. This section is where we attract the attention of potential candidates and sell the role.

What you'll do

• Be part of a high-performing, inclusive culture that values fresh thinking and collaboration
• Have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together
• Perform medical review and clarification of Trial related (AE's) & Post marketing Adverse Events (ADR's) including narrative content, queries
• Maintain awareness of medical-safety-regulatory industry developments to participate in trainings, workshops, product transitions, audit preparations
• Support audits and inspections for case processing & medical review aspects

What you need

• 3–4 yrs of experience
• Pharmacovigilance
• SOP writing
• Communication
• MBBS