Department: CMRQ (Clinical Medical Regulatory and Quality) Location: Beijing   The position •    Handle adverse events and other safety-related reports for all NN products; •    Support the PV operational processes ensuring compliance with NN procedures and regula-tory requirements; •    Support other pharmacovigilance operations.

  Qualifications •    Master's degree or above of clinical medicine, pharmacy or relevant; •    Min 6 years' experience in pharmaceutical industry or related industry, like medical devices or healthcare industry; •    Min 5 years in pharmacovigilance function; •    Familiar with China, EU, ICH pharmacovigilance legislation; •    Fluency in both written & spoken English; •    Customer orientation & good communication; •    Problem solving & pressure taken.

  About the department In CMRQ, we commit to bringing our products to Chinese market with the fastest speed and top quality, and applying the most scientific way to communicate our products' benefits to our customers.

We have 6 team in CMRQ aming to portfolio evaluation and overall strategy; New product approval, Licence maintenance, Product localization; Clinical evidence trial operation Phase (I-IV, NIS); Multiple stakeholders' engagement (HA/KOLs/investigators) and Medical evidence generation/communication.

  We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.    At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world.

We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures.

We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in.

Together, we’re life changing.