Pharmacovigilance Associate

In this role, you will be responsible for performing case intake of Individual Case Safety Reports (ICSRs) from various sources such as patients, healthcare professionals, and literature. Your key responsibilities will include entering and updating safety data accurately in pharmacovigilance databases, conducting initial assessment and triage of reported adverse events, and assisting in coding medical terms using MedDRA. Additionally, you will ensure timely and compliant reporting of safety cases to regulatory authorities and support the preparation of safety narratives and case summaries under supervision. You will also review source documents for accuracy and completeness, assist with signal detection, and participate in ongoing safety monitoring activities. It is essential that you follow SOPs, GVP guidelines, and global regulatory requirements, and collaborate with cross-functional teams including clinical, regulatory, and quality departments as needed. Qualifications Required: - Prior experience in pharmacovigilance or drug safety is preferred - Knowledge of MedDRA coding is a plus - Familiarity with SOPs, GVP guidelines, and global regulatory requirements - Strong attention to detail and accuracy in data entry - Excellent communication and interpersonal skills - Ability to work effectively in a team environment About the Company: The company offers a range of benefits including cell phone reimbursement, provided food, health insurance, paid sick time, and Provident Fund. Additionally, the role offers the flexibility to work from home. Please note that this is a full-time, permanent position suitable for fresher candidates. The work location is in person.,