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.
Job Responsibilities - Develop and implement real world evidence strategy in China and Asia region, Support observational studies, improve interactions with key external stakeholders including authority and external experts. - Deliver study results per required time-line - Deliver real world evidence strategy as requested - Provide professional advice/trainings in a timely manner - High-quality critical reviews - Deliver high-quality literature review and document sections on time - Maintenance of an epi expert network in China - Generate high-quality regional evidence - Develop and implement communication plan
Job Requirements - Training in statistics/epidemiology, or a related field, with suggested alternatives as follows: - PhD or MD/PhD in statistics/epidemiology or a related field plus minimum of two (2) years of relevant experience in the healthcare industry (Pharma/Biotech preferred) or academia OR - Master’s degree (MS/MPH/PharmD) in statistics/epidemiology from an accredited institution with minimum of four (4) years of relevant experience in the healthcare industry (Pharma/Biotech preferred) or academia - Epidemiology methods background, statistical skills, and medical/pharmacological knowledge - At least two years’ experience in leading projects - Experience with healthcare claims and/or electronic medical record databases - Proficient ability to speak, read and write in English and Chinese - International exposure in daily business environment - Strong written and verbal skills and well-developed multi-cultural sensitivity - Proactive, responsible, and accountable - Able to work independently as well as in cross-functional groups - Recommends improvements and alternative solutions to resolve problems - Understanding of the drug development and commercialization process - Basic pharmacovigilance knowledge - Knowledge of, or experience with, Chinese RWE data sources - Familiarity with Chinese regulatory and reimbursement environment - Experience working with patient registry data
