As this role, you will take part in Pharmacovigilance (PV) activities.
DUTIES
- Perform China Local Pharmacovigilance (PV) daily work, including collection of local spontaneous cases (follow-up activities, if applicable), translation of National Medical Products Administration (NMPA) feedback line listings, translation of China domestic cases in Global database (Argus) and literature monitoring
- Perform local PV team document (e.g.: PSUR) preparation as per regulatory authorities’ request
- Perform local PV team communication with global PV team
- Perform other MA-PV work (e.g.: management of PV documents such as SIEAs, PV training, support meetings held by MA, and other administrative affairs), if needed
COMPETENCIES REQUIREMENTS
- Sufficient English and writing skills
- Familiar with Microsoft Office software (e.g.: Word, Excel and PowerPoint)
- High sense of responsibility
- Independent job working capability under coaching
- Detail-oriented
BACKGROUND REQUIREMENTS
- Bachelor’s degree or above
- Major in medicine, pharmacology, medical English, translation and etc.
- Able to work at least 3 days/week
Inclusion and Diversity
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.