Key Responsibilities:

1. Pharmacovigilance Activities:
   • Assist in monitoring and reporting adverse drug reactions and ensuring compliance with regulatory requirements.
   • Participate in the collection, analysis, and interpretation of safety data.
2. Data Management:
   • Maintain accurate records of all safety data and ensure timely reporting to the relevant authorities.
   • Support data entry and management activities related to pharmacovigilance.
3. Regulatory Compliance:
   • Ensure all activities are in compliance with local and international regulatory requirements.
   • Assist in the preparation and submission of regulatory reports.
4. Collaboration:
   • Work closely with cross-functional teams to ensure the smooth flow of safety-related information.
   • Liaise with healthcare professionals and other stakeholders to gather safety data.

Important Details:

• Selection Process: The selection will be based on an interview.
• Mode of Interview: Face-to-face
• Interview Rounds: HR Interview

How to apply

appplication link

Another Refrence

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