Career Category

Job Description

Main Tasks

•     Identifies, develops, and maintains collaborative relationships with current and future Medical Experts (MEs), Health Care Providers (HCPs), scientific experts, cooperative study groups and study sites

•     Implements Scientific Engagement Plans (SEPs) in line with local and regional medical strategy

•     Communicates complex evidence-based scientific information and research concepts to MEs and HCPs.  Communication is reactive unless disease state or on-label per local compliance regulations

•     Implements and disseminates high quality medical and scientific educational programs; gives clinical and scientific presentations at sites / hospitals

•     Delivers clinical and scientific presentations as needed

•     Responds to scientific inquires by HCPs in a timely manner

•     Ensures society engagement: MSL collaboration with local, national, and international congresses

•     Implements and disseminates high quality medical and scientific educational programs

•     Discusses scientific value messages, clinical outcome and patient benefits with MEs, hospital pharmacists, and local payers in close collaboration with payer and access group as appropriate

•     Captures competitive information according to Amgen's ethical standards

•     Provides feedback based on field interactions with MEs and HCPs and documents interactions in ALIGN

•     Supports Amgen sponsored research to ensure prioritization of trial site selection and feasibility across assigned territories

•     Involves in SIV, SIM, and subject recruitment/retention strategies

•     Understands trial/referral networks and identify enrollment barriers

•     Participates in investigator meetings as appropriate

•     Responds to requests for investigator sponsored research proposals

•     Delivers targeted internal training for selected topics (e.g. study update, congress news, latest scientific developments)

•     Contributes to qualitative and quantitative reports

•     Ensures conduct of work in line with compliance regulations

Qualifications

•     Advanced degree (e.g. MD, PharmD, PhD, DO) preferred or strong demonstration of equivalent combination of relevant educational and professional training

•     Minimum 3 years of experience as an MSL in multinational pharmaceutical company

•     Oncology TA (solid tumor) related experience preferred

•     Experience of launching new product/indication preferred

•     Willingness to travel; According to the guidance of company

•     Experience with clinical study management and conduct

•     Medical / scientific research experience

Knowledge and Skill

•     Scientific expertise in the therapeutic area, related products, disease state, and interested in latest discoveries

•     Solid understanding of country local health care system and decision-making, stays on top of changes

•     Good knowledge of clinical research, drug safety, legal and compliance environment

•     Demonstrates strong project management and presentation skills

•     Knowledge of value messages, clinical outcomes and patient benefits for the products

•     Knowledge of commercialization and business practices

•     Willingness to continuously expand medical, scientific, market, and industry knowledge

•     Good communication skills and collaboration with internal and external stakeholders