Associate TA Head Medicine - INFL (Shanghai, China, Shanghai)

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

•    Build and lead a high-performing Medical Affairs and MSL team

•    Collaborate with TA Head to develop and execute medical strategy and evidence generation plans.

•    Provide medical leadership for new product launches and lifecycle management.

•    Gather market feedback and work with commercial teams to address gaps between business goals and external expert expectations; manage risks and develop contingency plans.

•    Represent local needs in the Global Medical Team.

•    Drive implementation of Medical Affairs plans, including engagement, collaboration, education, publications, and training

•    Strengthen external stakeholder networks and guide annual planning for MA and MSL teams

•    Lead pre-launch training on disease and patient journey.

•    Drive and execute medical strategy, ensuring successful product launches and lifecycle management.

•    Ensure effective delivery of medical plans and evidence generation

•    Build strong talent pipeline, develop key team members.

Qualifications

•    Master’s degree or above (MD or PhD in medicine-related field preferred).

•    At least 8 years’ experience in the medical department of multinational companies. 3-5 years in a position equivalent to medical advisor in the pharmaceutical industry.

•    Solid therapeutic area knowledge in target assets/products.

•    Strong understanding of medical affairs strategy, evidence generation, and product lifecycle management.

•    Ability to build networks with external experts, medical associations, academic centers, and regulators.

•    Experience in leading medical engagement activities, scientific collaboration, and medical education.

•    Familiarity with local post-marketing trials and investigator-initiated studies.

•    Knowledge of compliance, regulatory requirements, and scientific publication processes.

•    Proficient in both English and Mandarine

]]>