¢ºÀÓ»óÀÇÇÐ srManager (¼ö¼®)
[´ã´ç¾÷¹«]- Manage multi-disciplinary clinical trial teams to ensure all trial deliverables are met according to timelines, budgets, quality, and operational procedures. Manage clinicaltrial meetings, report study progress and issues, and provide resolution and action plans if necessary.- Accountable for clinical trial protocols and related documents. Contribute to the development/review of study related documents, plans, and processes. Prepare/review trainingmaterials and presentations related to the planning and conduct of the trial(s).- Accountable for the development, management, and forecast of study budgets/invoices
[ÀÚ°Ý¿ä°Ç]- ÇØ´ç ¾÷¹« ºÐ¾ß 10³â ÀÌ»ó- Çлç ÀÌ»ó- Àü°ø : Pharmacology, pharmaceutical science, and life sciences. Preferring Masters or Doctorate degrees- Thorough knowledge of GCPs, clinical trial design, regulatory processes, and global clinical development process- ÇØ¿ÜÃâÀå¿¡ °á°Ý »çÀ¯ ¾øÀ½ - MS PPT/Word/Excel ´É¼÷- English proficiency (written and verbal)
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Á÷¾÷Á¤º¸Á¦°ø»ç¾÷½Å°í¹øÈ£ J150002023003