Clinical Operations Manager-Minimum 7 years relevant experience in clinical researchClinical Operations Head-Minimum 11 years relevant experience in clinical researchCPM- PM °ü·Ã °æ·Â 1³â ÀÌ»ó Çʼö- Sr.CRA ÀÌ»ó ¶Ç´Â CPL, CPM À¯°æÇèÀÚ- ÇØ´çÁ÷¹« °æ·Â 4-5³â ÀÌ»ó Çʼö- ¿µ¾î ´ÉÅëÀÚ ¿ì´ëCPL¾÷°è °æ·Â 7³âÂ÷ ÀÌ»ó (monitoring °æ·Â ¸¸ 6³â ÀÌ»ó)¿µ¾î ´ÉÅëÀÚInter personal skill ¿ì¼öÇÑ ÀÚ & Good leadershipÀ» °¡Áø ÀÚSr.CRA, CRA- ±¹³» ¹× ÇØ¿Ü ÀÓ»ó½ÃÇè monitoring,site management- Sr.CRA ÇØ´çÁ÷¹« 5³âÀÌ»ó
QC of documents(TMF QC), QC visit, Coaching and training, etc*Minimum 5 year experience in clinical research in healthcare, pharmaceutical and/or CRO industry or minimum 4 year direct experience as monitor in clinical studies with good performance
- ¿µ¾î´ÉÅëÀÚ- Good presentationskills, use of computer/technology- Minimum 5 years working in CRO / pharmaceutical industry- Good communication, negotiation and analytical skills and able to makerecommendations to projectteams
* Having minimum of 5 years' experience in clinical medicine, in addition to 2 years' clinical trials experience as an investigator or in the Pharma, CRO, or Biotech industry will be preferred.
- Minimum bachelor degree (major in nursing, pharmacy, or other science-related background) from a recognized institution,and/or equivalent combination of training and experience- Minimum 5~6 years regulatory writing experience in clinical research, in healthcare, pharmaceutical CRO industry and/or related industry - Qualified candidates must have experience writing protocols and protocol amendments, clinical study reports, investigator brochures, and all types of regulatory agency submissions
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