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Amgen RML in Chengdu, China

Responsiblities:

Establish and maintain an in-depth scientific and clinical understanding in the area of

oncology for Amgen portfolio and pipeline

. Engage in scientific exchange with healthcare professionals to communicate and

advance the scientific communication platform, as aligned with pipeline goals and

objectives

. Communicate complex, cutting edge, scientific information and research concepts to

healthcare makers, including but not limited to, those at Centers of Education and

Research

. Identify, develop, and maintain collaborative relationships with current and future

thought leaders.

. Coordinate and communicate activities around opinion leaders with other Amgen field

based staff

. Make clinical and scientific presentations to healthcare audiences

. Identify / recommend sites for Amgen clinical trials in conjunction with and when

required by Development Operations

. Deliver site or regional investigator meetings in support of study rationale, trial

enrollment and/or subject retention

. Collect and communicate competitive intelligence within Amgen’s competitive

intelligence guidelines

. Manage the field activities related to the submission and execution of Investigator

Supported Studies (ISS) in line with Amgen’s existing policies

. Support reimbursement efforts by presenting clarity around clinical and scientific

information supporting therapeutic decisions in patient care.

Deliverables:

. Opinion leader scientific exchange

. Speaker development

. RML led regional educational programs

. Clinical study support

. Market access support

Basic Qualifications Selection Criteria (minimum qualifications):

. MD, PharmD or PhD is required

. Fluent in Chinese (Mandarin) and English

. Prior Medical Liaison experience is preferred

Preferred Qualifications & Preferred Requirements

. Established relationship with scientific thought leaders, preferably in cardivascular area

. Exceptional communication skills

. Experience working within a cross-functional matrix team environment

. Solid organization and project management experience

. Strategic, analytical thinking and problem solving

. Good understanding of the drug commercialization process

. Understanding of commonly used clinical trial statistical concepts

. Use of customer relationship management software

. User of Office tools (Word, Excel, Powerpoint, MS Project, Outlook, and Access)

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