Job Description

About Human Pharmaceutical Business

With global presence, Boehringer Ingelheim has industry-leading expertise in medicine research and development. We are constantly developing the next generation of medical breakthroughs and 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 and central nervous system. In the future, we will accelerate the launch of more than 10 innovative medicines to meet the demand of Chinese patients.

Responsibilities

• Serve as a trust partner on Medical Engagement and Partnership to the Medicine TAs.
• ­Work with global and local stakeholders to facilitate strategic medical engagement initiatives and build supporting processes, frameworks, systems, and platforms.

­- Support effective collaboration between TAs and cross-functional partners, including Regulatory Affairs, Marketing, and Market Access, etc.

• ­ Work with global and local stakeholders to continuously improve key medical affairs processes and systems to enhance efficiency and effectiveness.

­- Support the Medicine TAs in the design and implementation of annual goals and target breakdowns.

­- Deliver accurate, consistent and comprehensive performance reports with forecast, and report performance to the governance board with pre-identified issues with potential solutions.

­- Establish and maintain a repository of best practices, templates, and tools for the medical team.

­- Consciously pay attention to new technologies, digital tools, and innovative approaches and actively apply them in the daily work.

­- Serve as TA expert in the field of medical governance and SOPs, and strengthen TAs’ compliance awareness continuously, develop and manage compliance mechanism or standard process for continuous improvement.

• Collaborate with Medical Quality team to support on quality control of key medical delivery outcomes, including target setting and progress tracking.

­- Work with Audit, compliance review or any other projects as required.

­- Identify and mitigate compliance risks within the TAs.

Qualifications

• Master degree or above; MD or Master Degree of pharmacology, medicine or related area, Ph.D. or MBA is preferred;
• Minimum 2 years working experience in medicine or project management function, or proven experience in a medical excellence, medical operations, or medical strategy role.
• Excellent project management skills and financial planning and managing experience
• Knowledge of Compliance/Data Transparency/Conflict-of-Interest regulated work environments
• Excellent communication skill and strong leadership in cross-functional groups (internal and external)
• Fluent in English & Chinese