Medical Science Liaison (CV)
AmgenSouth korea - seoulUpdate time: March 10,2022
Job Description

Career Category

Medical Affairs

Job 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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