[ÀÌÈñÁ¤] ¿ÜÀÚÁ¦¾à»ç-CRA °æ·Â 1³â~3³â ¸ðÁý

Date 02/09/2010   Hits 1278

1. ÀÇ·Ú»ç: ¿Ü±¹°è Á¦¾à»ç

2. ¸ðÁý ³»¿ë : ¿ÜÀÚÁ¦¾à»ç-CRA °æ·Â 1³â~3³â ¸ðÁý

¢Ã Position : ÀÓ»ó ÀÇÇÐºÎ¼Ò¼Ó -(Á¤±ÔÁ÷)
* ¾÷¹«³»¿ë
- Conduct clinical trials monitoring and site management
- Conduct post-marketing surveillance (PMS) monitoring and management
- Contact relevant department of KFDA, investigators, pharmacists, and hospital IRBs.
- Contact relevant persons of HQ with conduct of clinical trials
- Safety monitoring and reporting to health authority and internal safety manager
- Management outsourcing regarding PMS and others
- Train PSRs with PMS procedures and medical background
* ÀÚ°Ý¿ä°Ç
- University graduate, pharmacist or major in Pharmacy or Nursing
- Minimum 1 years experience as a CRA
- Full knowledge of regulations (e.g., ICH-GCP, SOP, and local laws and regulations)
- Capability of communicating the chemistry, toxicology, pharmacology, and clinical pharmacology
- Capability of commanding respectful attention and cooperation of investigators to maintain activities
- Capability of communication with Health Authority and HQ effectively and efficiently
- Good command of written and spoken English

¢Ã ¿¬ºÀ¼öÁØ ¹× º¹¸®ÈÄ»ý : ÃßÈÄ ÇùÀÇ °¡´É

¢Ã ±Ù¹«Áö : ¼­¿ï

¢Ã Á¦Ãâ¼­·ù: ±¹¹® ¹× ¿µ¹® À̷¼­ ¹× °æ·Â±â¼ú¼­,Àڱ⠼Ұ³¼­

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

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