[°ûÁöÇý] Regulatory Submissions Associate(°æ·Â 2³âÀÌ»óÀÚ ¸ðÁý)

Date 11/23/2010   Hits 1393

1. ÀÇ·Ú»ç: ¼¼°è ÃÖ´ë ±Û·Î¹ú CRO

2. ¸ðÁý ³»¿ë : Regulatory Submissions Associate(°æ·Â 2³âÀÌ»óÀÚ ¸ðÁý)

- ÇÐ»ç ¶Ç´Â ¼®»ç ÀÌ»ó ¿ì´ë
- ¾àÇÐ,Á¦¾àÇÐ,¼öÀÇÇÐ,À¯Àü°øÇÐ,»ý¹°ÇÐ,»ý¸í°øÇÐ µî °ü·Ã Àü°øÀÚ ¿ì´ë
-Responsible for the timely preparation of submissions (IND/CTA and others) or of parts thereof to Regulatory Authorities, working to a high standard with minimal supervision.
-Interacts with Regulatory Authorities and with clients to support regulatory activities.
- Proactively interacts with other groups and with clients to provide guidance regarding Regulatory Authority requirements and project timelines and requirements.
- It is the responsibility of the Senior Regulatory Associate to prepare documents to the required standard and to maintain awareness of current regulatory standards related to submissions for drug and biologic products. May have supervisory responsibilities.

¢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