Our strategic partner, headquartered in Singapore, is the foremost distributor of medical aesthetics and dermatological technologies in Southeast Asia and China.
Location: Ho Chi Minh City, Vietnam
Job Responsibilities
- Monitor, collect, assess, and report adverse events from healthcare professionals, patients, and other relevant sources.
- Ensure pharmacovigilance reports are submitted to regulatory authorities within required timelines.
- Maintain and manage the Pharmacovigilance System Master File in accordance with regulatory requirements when applicable.
- Develop and implement risk management plans for products available on the market.
- Analyze benefit-risk profiles and provide safety-related recommendations to management and regulatory stakeholders.
- Ensure full compliance with local and international pharmacovigilance regulations and guidelines.
- Continuously update knowledge of global pharmacovigilance regulations and industry best practices.
- Analyze adverse event data to identify potential safety signals.
- Conduct benefit-risk evaluations and communicate safety findings to relevant stakeholders.
- Ensure accurate collection, storage, and reporting of safety data throughout the pharmacovigilance lifecycle.
- Utilize pharmacovigilance databases and systems to manage and track safety information.
- Collaborate with internal teams including medical, regulatory, and clinical functions to support integrated safety management.
- Communicate safety information effectively to internal stakeholders, health authorities, and healthcare professionals.
- Provide training to internal staff on pharmacovigilance procedures and adverse event reporting requirements.
- Prepare for regulatory audits and inspections related to pharmacovigilance activities.
- Ensure ongoing internal audits of the pharmacovigilance system to maintain regulatory compliance.
Job Requirements
- Bachelor’s degree in Pharmacy, Medicine, or a related scientific discipline is required.
- Advanced academic qualifications such as a Master’s degree or Ph.D. in relevant fields are preferred.
- Additional certifications or formal training in pharmacovigilance or drug safety are advantageous.
- Up to three years of experience in pharmacovigilance or related areas such as clinical research or regulatory affairs.
- Understanding of adverse event reporting processes and safety databases.
- Knowledge of global pharmacovigilance guidelines and regulatory frameworks.
- Ability to perform safety data analysis, signal detection, and trend evaluation related to drug safety.
If you possess the required skills and experience and are ready to significantly contribute to the dynamic team, we warmly welcome your application at tham.nguyen@peoplewise.vn or application@peoplewise.vn.
About PeopleWise Vietnam:
PeopleWise Vietnam was founded with the mission of positively impacting our community by improving the quality of the labor force, addressing workforce dynamics, and enhancing its effectiveness. During our initial phase, we provided solutions and human resources consulting services to our partners worldwide, including workforce advisory, organizational diagnosis, career transition, training services, talent management, and staffing solutions that align with each organization’s values and vision, driving business success.
Visit us at our website: https://peoplewise.vn/
To apply for this job email your details to tham.nguyen@peoplewise.vn