Pharmacovigilance Associate

A pharmacovigilance associate ensures compliance with applicable regulations or standard operating procedures; specialises in drug safety management, clinical trials and medical supervision. - Responsible for conducting, monitoring or reporting regular pharmacovigilance developments and supervising the processes related to ensuring drug effectiveness and...

**Primary Responsibilities**: 1. General Responsibilities and Regulatory Compliance: - Execute pharmacovigilance activities as nationally required (e.g. adverse event management, expedited and periodic reporting, risk management and creation and maintenance of the Pharmacovigilance System Master File). - Monitor national pharmacovigilance legislation. -...

We are seeking a highly motivated and detail-oriented recent graduate to join our Pharmacovigilance team as an Entry-Level Pharmacovigilance Associate. This is a fantastic opportunity to begin your career in the pharmaceutical industry and contribute to the safety monitoring of our products. You will gain hands-on experience in various aspects of...

Basic understanding of pharmacovigilance processes and regulatory requirements. - Strong attention to detail and accuracy in data entry and report preparation. - Ability to work in a team and follow instructions from senior professionals. - Proficiency in MS Office (Word, Excel, PowerPoint). - Good written and verbal communication skills. - Eagerness to...

**Primary Responsibilities**: 1. General Responsibilities and Regulatory Compliance: - Execute pharmacovigilance activities as nationally required (e.g. adverse event management, expedited and periodic reporting, risk management and creation and maintenance of the Pharmacovigilance System Master File). - Monitor national pharmacovigilance legislation. -...

**Key responsibilities of a Pharmacovigilance Associate**: - **Case Processing**:Receiving, reviewing, and processing individual case safety reports (ICSRs) from various sources like healthcare professionals, clinical trials, and patients. - **Data Entry and Management**:Accurately capturing adverse event details into specialized safety databases, including...

**Primary Responsibilities**: 1. General Responsibilities and Regulatory Compliance: - Execute pharmacovigilance activities as nationally required (e.g. adverse event management, expedited and periodic reporting, risk management and creation and maintenance of the Pharmacovigilance System Master File). - Monitor national pharmacovigilance legislation. -...

**Responsibilities**: - Process and assess individual case safety reports (ICSRs) - Enter and manage safety data in databases - Perform quality checks on safety reports - Assist in preparing regulatory reports (e.g., PSURs, DSURs) - Support signal detection and risk management activities **Skills Required**: - Knowledge of pharmacovigilance regulations...

A career in pharmacovigilance provides good prospects with generation of new drugs evey day. Pharmacovigilance is the process of collecting, reseraching, monotoring, evaluating and assessing information delivered directly or indirectly from patients. **Job Types**: Full-time, Fresher **Salary**: ₹15,000.00 - ₹25,000.00 per month **Benefits**: - Cell...

TCS is hiring PharmacovigilanceJob Location: PuneExperience Range : 2 - 6 YearsEducational Qualification(s) Required: Any Life Science graduateRequired Skillsets:Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data.Be fully competent to perform all steps within the...