Pharmacovigilance Associate

**Key Responsibilities**:

- **Case Management**:

- Receive, document, and assess adverse event reports from various sources, including healthcare professionals, consumers, and regulatory authorities.
- Ensure accurate and timely data entry of adverse event information into the safety database.
- Conduct thorough case investigations and follow-up activities to obtain missing information.
- **Signal Detection and Evaluation**:

- Assist in the identification of potential safety signals through the analysis of aggregated safety data.
- Contribute to the evaluation of safety signals by reviewing relevant literature and data.
- **Regulatory Compliance**:

- Stay abreast of relevant pharmacovigilance regulations and guidelines.
- Assist in the preparation and submission of periodic safety reports to regulatory authorities.
- **Collaboration and Communication**:

- Collaborate with cross-functional teams, including Clinical Development, Regulatory Affairs, and Medical Affairs.
- Communicate effectively with internal and external stakeholders regarding safety-related issues.
- **Quality Assurance**:

- Participate in internal and external audits related to pharmacovigilance activities.
- Ensure compliance with internal Standard Operating Procedures (SOPs) and industry best practices.

**Qualifications**:

- Bachelor's degree in pharmacy, life sciences, nursing, or a related field.
- Strong attention to detail and excellent organizational skills.
- Effective communication and interpersonal skills.
- Ability to work independently and collaboratively in a team environment.

**Job Types**: Full-time, Permanent, Fresher

**Salary**: ₹250,000.00 - ₹350,000.00 per year

**Benefits**:

- Health insurance
- Internet reimbursement
- Paid time off
- Provident Fund

Schedule:

- Day shift
- Weekend availability

Supplemental pay types:

- Performance bonus
- Quarterly bonus

**Education**:

- Bachelor's (preferred)

Work Location: In person