Job Information
Amgen Sr. MA- EVENITY in Shanghai, China
Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people’s lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world’s leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.
Role Summary
The Sr. MA- EVENITY. Working with the supervisor, this position will serve as the point of contact with other Amgen China function teams and with Amgen global teams and medical activities in bone health therapeutic area (TA). As such, this position is responsible for providing medical insights into the relevant TA and/or specific molecules to the China teams and the global teams to inform medical affairs strategies for China, and for executing the activities accordingly
Responsibilities:
Working on the planning, data generation and communication for China focused therapeutic areas
Participating in/conducts Local Advisory Board Meetings, Investigator Meetings, Expert Panels and other medical activities
Establishing and maintaining relationship with key investigators, thought leaders, and professional organizations in the relevant therapeutic areas in the Chinese medical community
Developing and executing the China medical plan and medical activities for the product(s) in accordance to internal and external regulations
Providing therapeutic area and/or product specific medical education, ensuring consistency of medical content and scientific messages across various tools and materials
Supporting China local study team in participation and completion of global development studies in China; visiting selected KOL’s and study groups for strategic discussions and protocol development; providing input into site selection for Amgen-sponsored studies; developing and executing better recruitment strategies in conjunction with China local study teams; providing local support for medical questions, feasibility and trial strategy
Overseeing in-sourced/outsourced medical programs and logistics
Supporting China regulatory and ethics approvals for study protocols
Basic Qualifications
MD, PharmD or PhD is required
Fluent in Chinese (Mandarin) and English
Prior Medical Liaison experience is preferred
Preferred Qualifications
Established relationship with scientific thought leaders, preferably in Psoriasis area
Medical and/or scientific expertise
Fluency in English, both oral and written communications
Strong communication and presentation skills
Continuously expanding medical and scientific knowledge as well as overall product related knowledge
Certain level of clinical research knowledge, such as: study design, study evaluation, medical writing skills, expert panel conduct, symposium and workshop management, KOL management
Strong customer orientation; science-based
Ability to work in a cross-functional team (e.g., Commercial, Clin Development, Regulatory, Safety, etc.)