- Lead the team to conduct post marketing trials/IITs to obtain the new evidence as the growth engine to leverage post-marketing product’s continuous development in China in compliance with GCP. Concept sheets, synopsize, protocol and preparation of other trial initiation documents trial approval at the required level (Local, Regional, Glob-al) and review/approval of amendments budget preparation, review, approval and tracking, ensure payment is made according to pre-defined payment schedule in the contract CSR and publications within planned timeline Define IIT Strategies and responsible for oversee and manage the whole process of execution of IIT including contract, payment and publication in alignment with GCP, Local regulations, NVS SOP Oversee and manage scientific project including but not limited to animal and in vitro studies (investigator initiated pre-clinical studies) - Supervise or responsible for Medical Grants and ensure it is in compli-ance with NVS policies.
Advanced scientific degree (PhD,PharmD,or MD); Excellent oral and written communication skills. a minimum of 7 years Oncology experience. - Proficient level of understanding in pharmaceutical business. - Experience in driving the development of medical strategies / key scientific message platforms without supervision. - Broad experience in planning and executing advisory boards, clinical trials, symposia, medical education materials and scientific posters/abstracts. - Ability to provide strategic insight into scientific expert development activities, publication planning plus developing medical education materials and programs that support product launches in oncology. - People managment experience - Excellent interpersonal skills. Ability to work with internal and external stakeholders. - Ability to travel around 20% of time.