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• Make medical plan and strategies in alliance with global medical strategies and local brand strategies.
• Plan, design, oversee execution and report clinical trials in accordance with ICH- GCP/KGCP guidelines, Roche SOPs and any relevant local regulation.
• Track actual expenditure against budget to facilitate effective control of project expenditures.
• Bachelor degree related to medical/pharma/science field or higher degree
• High level of understanding clinical trial activities
• Knowledge of ICH-GCP/KGCP, Roche SOPs and local regulatory requirements.
• Understanding in pharmaceutical environment, regulation and business
• Good verbal and written English knowledge and skill
• At least 3 years of work experience in the pharmaceutical industry and a medical environment is desired
• Experience in oncology is preferred
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