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About the Role

Contribute to maximizing product value and patient outcomes through medical and scientific engagement activities with external customers in the oncology field. Conduct Scientific Interviews and Scientific Exchanges with disease area experts from late-stage development to gather insights for appropriate post-launch use. Explore unmet medical needs for products through proactive and continuous engagement with specific physicians, advisory board meetings, and published papers. Synthesize gathered insights and collaborate with external stakeholders to plan long-term medical activities and project plans.

Responsibilities

Maximize product value through scientific exchange by achieving scientific objectives in the responsible therapeutic area based on GBP/ICP.
Provide information to meet medical and scientific needs and research support from External Experts (EE) and other medical personnel in the responsible therapeutic area.
Build activity plans based on GBP/ICP.
Identify and appropriately revise EEs in the responsible therapeutic area.
Develop appropriate EE engagement plans based on GBP/TA strategy in the responsible therapeutic area.
Record and execute EE engagement plans aligned with GBP/ICP.
Conduct Scientific Interviews/Scientific Exchanges to gain scientific insights on responsible products from EEs and create appropriate content.
Share scientific insights, including the latest information from congresses, with relevant departments to develop strategies and action plans.
Support the planning and organization of advisory boards for execution in the responsible therapeutic area and implement scientific meetings.
Build and sustain positive relations with target EEs throughout the product life cycle via regular contact and communication.
Utilize digital tools in customer engagement.
Manage budgets and leave records for responsible activities.
Provide support for IIS and data building.
Create new scientific data considering feasibility, scientific appropriateness, and ethics to fill data gaps and unmet needs.
Support clinical/non-clinical IIS as a liaison based on requests.
Provide scientific data on approved/unapproved/off-label products based on customer requests.
Create appropriate content based on requests and scientific questions from EEs and other medical personnel, and provide appropriate information after full approval within the responsible therapeutic area.
Provide research result data slides to speakers and speaker candidates based on requests.
Attend speaker trainings to conduct scientific content training and answer questions based on requests.
Conduct MR training to improve the knowledge level of MR, based on requests from the training department.
Understand and comply with regulations and industry rules (promotional codes, fair competition rules, privacy, data collection/storage, etc.) as well as related SOPs.
Act according to social norms and the company's code of conduct with full awareness as a responsible employee.

Requirements

Experience in Oncology area as an MSL, Medical Affairs, or Clinical Development (CRA, clinical trial manager, etc.).
Experience with product launches in a pharmaceutical company is preferable.
Experience interacting with EEs in the relevant field of expertise is desirable.
Excellent communication skills with EEs are preferable.
Strong logical thinking and problem-solving skills are preferable.

Skills

Logical thinking
Problem-solving
Communication

Education Level

PhD
MSc
Pharmacist