1. ÀÇ·Ú»ç: ¼¼°èÀûÀÎ À¯¸í CRO
2. ¸ðÁý ³»¿ë : Clinical Research Associate °æ·Â 1³âÀÌ»óÀÚ ¸ðÁý
¢Ã Job Responsibilities(Á¤±ÔÁ÷) : Çѱ¹ ±Ù¹« 7¸í ä¿ë ¿¹Á¤
- 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.
- 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, ¿¬ºÀÀÌ»óÀ¸·Î ÃßÈÄ ÇùÀÇ °¡´É/ ÁÖ5ÀÏÁ¦
¢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
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