Boehringer Ingelheim oc jobs (salary & requirements)

About Human Pharmaceutical Business
With global presence, Boehringer Ingelheim has industry-leading expertise in medicine research development. We are constantly developing the next generation of medical breakthroughs successfully delivering innovations to meet the medical needs of the patients we serve in the following key areas of interest: cardiovascular, respiratory, metabolic diseases, immunology, oncology central nervous system. In the future, we will accelerate the launch of more than 10 innovative medicines to meet the demof Chinese patients.
Responsibilities
• Provide scientific inputs from safety perspectives in key milestones across asset lifecycle including but not limited to the briefing book, IB, CTP, CTR, local label, ICSRs, etc.
• Lead the local RMP strategy ensure on-time high-quality local RMP preparation, implementation evaluation according to local regulatory requirements.
• Generate local safety reports to Health Authority per regulations like safety summary flicense renewal, fatal/cluster case investigation reports, etc.
• Review the local safety with summary per requirements keep necessary communication with relevant stakeholders.
• Provide scientific inputs from safety perspective on the post-marketing studies (e.g. ONIS, IIS, ECR) contribute to the development implementation fthe local PASS per local regulations
• Deliver PV knowledge asset safety profile training to internal external customers as needed.
• Support LPSL on maintenance of local PV system contributes to the PV Quality system
Qualifications
• Master’s degree above in clinical medicine
• 3+ years of pharmaceutical industry/hospital experience, pharmacovigilance clinical development/medical affairs role is a plus
• Excellent medical judgment scientific analysis skills
• Strong communication influencing skills
• Cross-functional collaboration
• Strategic thinking project management
• Risk assessment capabilities
• Good Commof English Chinese