[ÀÌÈñÁ¤] ¿Ü±¹°è, CRA(°æ·Â 1³âÀÌ»ó), Sr.CRA(°æ·Â 3³âÀÌ»ó) ¸ðÁý |
Date 11/06/2008 Hits 1126 |
1. ÀÇ·Ú»ç: À¯¸í ¿Ü±¹°è CRO
2. ¸ðÁý ³»¿ë : CRA ¹× Senior CRA ¸ðÁý
¢Ã Position : CRA(°æ·Â 1³âÀÌ»ó), Sr.CRA(°æ·Â 3³âÀÌ»ó) -Á¤±ÔÁ÷ - 3¸í ä¿ë ¿¹Á¤
¢Ã Job Responsibilities:
- Oversees the progress of a Clinical Trial, ensuring that it is conducted, recorded and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) and the applicable Regulatory requirements.
- Administer protocol and related study training to assigned site.
- Establish regular lines of communication with sites to manage ongoing project expectations and issues.
¢Ã Qualifications Required:
- Bachelor Degree in Science, with a major in Pharmacy, Biological / Life Sciences or Nursing from a recognized tertiary institution
- Minimum 1 year of clinical monitoring experience in the pharmaceutical / CRO industry for CRA.
- Minimum 3 year of clinical monitoring experience in the pharmaceutical / CRO industry for Senior CRA.
- Preferably with some experience in leading clinical teams in the region
- Good knowledge of drug development process, clinical trial monitoring procedures, medical terminology and GCP/ICH guidelines
- Excellent organizational and problem solving skills
- Strong written and verbal communication skills
- Good command of Enghis is a must
- Ability to travel when required and Be willing to travel 35-40% of the time
¢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: ÀÌÈñÁ¤
¿¬¶ôó : 02-567-7407,7408
À̸ÞÀÏ : yskim@jhhr.co.kr
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