1. ¼Ò¼Ó ÇìµåÇåÆà ȸ»ç¸í: Á¦ÀÌ¿¡ÀÌÄ¡¿¡ÀÌÄ¡¾Ë-JHHR /
ÁÖ¼Ò : ¼¿ï½Ã °³²±¸ ¿µµ¿´ë·Î 511, 30Ãþ 3001È£ (»ï¼ºµ¿, Æ®·¹À̵埿ö)
2. ¼Ò¼Ó ÇìµåÇåÆûç ȨÆäÀÌÁö: http://www.jhhr.co.kr
3. ¼Ò¼Ó ÇìµåÇåÆûç ȸ»ç ÀüȹøÈ£: 82-2-567-7407 (Á÷Åë)
4. ¼Ò¼Ó ÇìµåÇåÆûç ȸ»ç¿ë, À̸ÞÀÏ : jhkwak@jhhr.co.kr
5. Æ÷Áö¼Ç ÁøÇà ÇìµåÇåÅÍ¸í ¹× Á÷±Þ : °û Áö Çý ´ëÇ¥ ÄÁ¼³ÅÏÆ®
6. ÁøÇà Æ÷Áö¼Ç¸í(°£´Ü ±âÀç):
7. »ó¼¼ Æ÷Áö¼Ç ³»¿ë :
[±Û·Î¹úÁ¦¾à»ç] Medical Affairs Team¼Ò¼Ó, Phase 4 ÀÓ»ó½ÃÇè°ü¸®(PMS, IIS)´ã´ç, ÆÀ¿ø±Þ(Á¤±ÔÁ÷) ¸ðÁý
2. ÀÇ·Ú»ç : [±Û·Î¹úÁ¦¾à»ç]
¢Ã Position : [±Û·Î¹úÁ¦¾à»ç] Medical Affairs Team¼Ò¼Ó, Phase 4 ÀÓ»ó½ÃÇè°ü¸®(PMS, IIS)´ã´ç, ÆÀ¿ø±Þ(Á¤±ÔÁ÷) ¸ðÁý
QUALIFICATION
- Excellent organizational skill, ability to prioritize and handle multiple tasks, negotiation skills and medical knowledge and ability to learn relevant business area
- 4+ years related experience of project overall management including outsourced people management and budget projection in pharmaceuticals (including minimum 3 + yrs experience of study project management and regulatory engagement with MFDS are mandatory)
- Must have full cycle experience
- University degree or higher in relevant field of science (Pharmaceuticals, nursing, biology,
epidemiology etc) Or an equivalent combination of education and experience
- Strong knowledge and skills in developing core documents in study and regulatory required supplementary evidence.
- Proactive, Interpersonal, decision-making issue resolution skills are required
- Good communication, negotiation presentation skill
- Comprehensive knowledge of clinical development process relevant regulations (e.g., GCP, SOP, local regulations)
- Publication (authorship) experience preferred.
- Native in Korean, Fluent in English
¢Ã ¿¬ºÀ¼öÁØ ¹× º¹¸®ÈÄ»ý: Çö, ¿¬ºÀ ÀÌ»ó ÃßÈÄ °æ·Â¿¡ µû¶óÇùÀÇ °¡´É / ÁÖ5ÀÏÁ¦ / 4´ë º¸Çè µî
¢Ã Á¦Ãâ ¼·ù : ±¹¹® À̷¼ ¹× °æ·Â ±â¼ú¼ ¶Ç´Â ¿µ¹® CV
¢Ã ´ã´çÀÚ: °ûÁöÇý
¿¬¶ôó : 82-2-567-7407(Á÷Åë)
À̸ÞÀÏ : jhkwak@jhhr.co.kr |