1. ÀÇ·Ú»ç: ¿ÜÀÚ CRO
2. ¸ðÁý ³»¿ë : ¿ÜÀÚ, Senior Clinical Research Associate ¸ðÁý
¢Ã Position : Á¤±ÔÁ÷ - Sr.CRA
¢Ã Responsibilities :
- Participate in site selection process, perform evaluation and make recommendation for trial inclusion.
- Facilitate communication between sites and line functions and increase value proposition to investigators.
- Facilitate preparation and collection of site level documents, resolve problems as required.
- Execute site initiation and training.
- Manage data at the site, resolve technical and content issues
- Implement closeout activities.
- Complete and generate study monitoring reports.
- Act as a mentor to new associates.
- Ensure site activities in line with milestones and project timelines.
- Ensure compliance of GCP, ICH and SOP.
- Review and manage study budgets.
¢Ã Requirements :
- Bachelor¡¯s level degree in life sciences or pharmacy
- 3 to 4 years of Oncology clinical monitoring experience
- Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
- Ability to lead and mentor a team
- Ability to work independently in a fast-paced environment
- Strong communication, interpersonal, and organizational skills
- Must demonstrate good computer skills
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¢Ã ´ã´çÀÚ: °ûÁöÇý
¿¬¶ôó : 02-567-7407,7408
À̸ÞÀÏ : yskim@jhhr.co.kr
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