Medical Science Liaison (CV)
AmgenSouth korea - seoulUpdate time: March 10,2022
Job Description
Career Category
Medical AffairsJob Description
Medical Science Liaison
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: 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
- Involved in SIV, SIM, and subject recruitment/retention strategies
- Understand trial/referral networks and identify enrollment barriers
- Participates in investigator meetings according to approved strategy
- 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. PharmD, PhD, MD) 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
- Cardiovascular TA related experience preferred
- Willingness to travel
- Experience with clinical study management and conduct
- Medical / scientific research experience
Knowledge
- Scientific expertise in the therapeutic area, related products, disease state, and interested in latest discoveries
- Has 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
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