Roles and

Responsibilities:

- Process adverse event reports (AERs) received from healthcare providers, patients, or other sources in accordance with regulatory requirements.
- Conduct thorough reviews of AERs to identify potential safety signals and determine whether they meet criteria for reporting to regulatory authorities.
- Collaborate with cross-functional teams to resolve issues related to AER processing, including data entry errors, missing information, or discrepancies.
- Maintain accurate records of all AERs processed, ensuring compliance with company policies and procedures. Job

Requirements:

- 1-3 years of experience in pharmacovigilance or a related field such as clinical trials or medical affairs.
- Solid understanding of case processing principles and regulations governing pharmaceutical industry operations.
- Proficiency in managing large volumes of data accurately and efficiently using electronic systems like CRM software.

📌 Drug Safety Physician (Bengaluru)
🏢 Indegene
📍 Bengaluru