
Drug Safety Associate
2 weeks ago
Responsibilities:
- Receive and process adverse event reports from various sources, including healthcare professionals, consumers, and clinical trials.
- Conduct initial assessment of reported adverse events to determine seriousness, expectedness, and causality.
- Enter adverse event data into safety databases accurately and in a timely manner, ensuring compliance with regulatory requirements and internal procedures.
- Perform case processing activities, including narrative writing, coding, and follow-up with reporters for missing or incomplete information.
- Conduct literature searches to identify relevant safety information and contribute to signal detection activities.
- Assist in the preparation and submission of expedited and periodic safety reports to regulatory authorities.
- Participate in safety surveillance activities, including trend analysis and periodic safety reviews.
- Collaborate cross-functionally with Clinical Development, Regulatory Affairs, Medical Affairs, and other stakeholders to ensure timely and appropriate risk management strategies.
**Job Types**: Full-time, Fresher
**Salary**: ₹24,000.00 - ₹27,000.00 per month
**Benefits**:
- Health insurance
- Provident Fund
- Work from home
Schedule:
- Day shift
- Monday to Friday
**Experience**:
- total work: 1 year (preferred)
Work Location: Remote
**Speak with the employer**
+91 8237213453
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