[°ûÁöÇý] ½Å»ý±Û·Î¹úCRO,PM ¶Ç´Â CRM °æ·Â 5³âÀÌ»óÀÚ ¸ðÁý

Date 07/11/2011   Hits 1006

1. ÀÇ·Ú»ç: ½Å»ý ±Û·Î¹ú CRO - Set Up Áß

2. ¸ðÁý ³»¿ë : Project Manager / Clinical Research Manager °æ·Â 5³âÀÌ»óÀÚ ¸ðÁý (Á¤±ÔÁ÷)

¢Ã Qualifications/ Requirements:
- Masters's degree in a health care or other scientific discipline or equivalent educational qualification
- Additional management qualification / advanced course / degree in Clinical trials is an added advantage.
- Strong verbal and Written english communication
- Excellent organizational and problem-solving skills
- Effective time management skills
- Ability to manage competing priorities

¢Ã Essential Responsibilities:
- Responsible for all the project deliverables of Clinical Trials.
- Assign, train and manage resources.
- Manage study budgets
- Ensure compliance in terms of ICH-GCP, Protocol, and other applicable regulations.
- Follow up with KFDA. Past Experience in preparation of regulatory dossier and getting trial approval from KFDA will be viewed very positively.
- Co-monitoring with CRAs.

¢Ã ¿¬ºÀ¼öÁØ ¹× º¹¸®ÈÄ»ý: Çö, ¿¬ºÀ ÀÌ»ó ÃßÈÄ °æ·Â¿¡ µû¶ó ÇùÀÇ °¡´É

¢Ã ±Ù¹«Áö : ¼­¿ï

¢Ã Á¦Ãâ¼­·ù: ±¹,¿µ¹® À̷¼­ ¹× »ó¼¼ °æ·Â±â¼ú¼­¿Í Àڱ⠼Ұ³¼­

¢Ã ÁøÇàÀýÂ÷ : 1Â÷ ¼­·ù ÀüÇü- 2Â÷ ¸éÁ¢ÀüÇü

¢Ã ´ã´çÀÚ: °ûÁöÇý
¿¬¶ôó : 02-567-7407,7408
À̸ÞÀÏ : yskim@jhhr.co.kr