¿Ü±¹°è Á¦¾à ȸ»ç
 ¸ðÁýºÎ¹®  Clinical Project Manager
 ¸ðÁýÀοø  0¸í
 ¾÷¹«³»¿ë  - Ensuring clinical trials are effectively executed and completed within budget,
timelines and meeting enrollment commitments as well as routine updating of clinical
systems. Pro-active trial management to identify challenges, develop effective
mitigation plans and to appropriately escalate and inform all relevant parties.
- Ensuring management of trials are done in compliance with ICH, GCP, local laws and
regulations. To maintain quality standards, the CPM is involved in additional protocol
specific training and might be supporting co-monitoring with a CRA. Providing country
specific guidance and oversight to CRO's where needed.
- Manage site pre-selection and validation process. Support local investigator meetings,
ensure contracts and applicable reg documentation is obtained prior to study start.
Facilitation of all aspects of IRB/ERC and Regulatory Agency submissions (including local IC).
PPOC for all logistical and operational issues and facilitate general communication.
- Oversee drug and clinical supplies management to ensure sites have timely availability
of required materials to avoid disruption of protocol deliverables
- Ensure clinical study site close-out in accordance with local regulations and ensure
dissemination of clinical trial results to the participating study investigators.
 Áö¿øÀÚ°Ý - CRA or CPM ¾÷¹« °æ·ÂÀÚ
- Good Command of English
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 ¸ðÁý±â°£  ~ 12. 2. 15 ±îÁö
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 ÀüÈ­¹øÈ£  02-597-1780
 ±âŸ»çÇ×  [Á¢¼ö¹æ¹ý] E-mail : jiko01@kohuman.com (À̸ÞÀÏ Á¢¼ö¸¸ °¡´É)
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 È¸»ç¼³¸í  ¿Ü±¹°è Á¦¾à ȸ»ç

ÃѰԽù°: 515 ÃÑÆäÀÌÁö: 18 ÇöÀçÆäÀÌÁö: 7
¹øÈ£ ¸ðÁýºÎºÐ °æ·Â ¿¬ºÀ ¸ðÁý±â°£ ÀÛ¼ºÀÏ Á¶È¸
335   QA(Quality Assurance) ´ã´ç 3³âÀÌ»ó Nego. ~ 12. 7. 10 ±îÁö 12-05-11 5092
334   Biostatistics & Data Managemen 10³âÀÌ»ó Nego. ~ 12. 5. 28 ±îÁö 12-05-11 5083
333   PV(pharmacovigilance) 4³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-05-11 5220
332   Finance Manager 10³âÀÌ»ó Nego. ~ 12. 5. 18 ±îÁö 12-05-07 4997
331   HR Manager 10³âÀÌ»ó Nego. ~ 12. 7. 20 ±îÁö 12-05-07 5040
330   ¿¬±¸¿ø ¸ðÁý 3³âÀÌ»ó Nego. ~12. 4. 30 ±îÁö 12-04-23 5119
329   HR Manager 7³âÀÌ»ó Nego. ~ 12. 4. 28 ±îÁö 12-04-16 5095
328   Clinical Project Manager 5³âÀÌ»ó Nego. ~ 12. 3. 31±îÁö 12-03-16 5182
327   Pharmacovigillance Specialist 3³âÀÌ»ó Nego. ~ 2012. 3. 24 ±îÁö 12-03-15 5088
326   QA Specialist 3³âÀÌ»ó Nego. ~ 12. 3. 24 ±îÁö 12-03-15 4964
325   Drug Product Manager 3³âÀÌ»ó Nego. ~ 12. 3. 20 ±îÁö 12-03-06 4926
324   Bioassay Scientist 3³âÀÌ»ó Nego. ~ 12. 3. 20 ±îÁö 12-03-06 5208
323   Product Manager 5³âÀÌ»ó Nego. ~12. 2. 18 ±îÁö 12-02-08 4921
322   (Sr) Business Research special 4³âÀÌ»ó Nego. ~12. 2. 14 ±îÁö 12-02-06 5008
321   Medical Science Liason Manager 8³âÀÌ»ó Nego. ~12. 1. 31 ±îÁö 12-01-16 5177
320   ÇØ¿Ü»ç¾÷ & ¶óÀ̼¾½Ì ´ã´ç ÀÓ¿ø 15³âÀÌ»ó Nego. ~12. 2. 15 ±îÁö 12-01-06 5117
319   CRA 2³âÀÌ»ó Nego. ~ 12. 1. 13 ±îÁö 11-12-30 5076
318   Çмú´ã´ç(½ÅÀÔ or °æ·Â) ½ÅÀÔ Nego. ~ 12. 1. 13 ±îÁö 11-12-30 4820
317   ½Å·Ú¼º º¸Áõ ´ã´çÀÚ(QAU) 2³âÀÌ»ó Nego. ~ 12. 1. 13 ±îÁö 11-12-30 5079
316   ¾à¹° ºÐ¼® ¿¬±¸¿ø/½ÅÀÔ ¹× °æ·Â 1³âÀÌ»ó Neg. ~ 12. 1. 13 ±îÁö 11-12-30 5125
315   Sr. Regulatory Affairs Special 7³âÀÌ»ó Nego. ~ 12. 2. 15 ±îÁö 11-12-20 5038
314   Clinical Project Manager 5³âÀÌ»ó Nego. ~ 12. 2. 15 ±îÁö 11-12-16 5105
313   Regulatory Affairs(Çã°¡/µî·Ï)-Á¦¾à,ÀÇ 3³âÀÌ»ó Nego. ~ 11. 12. 31±îÁö 11-12-08 5165
312   Planning & Admin. Manager 10³âÀÌ»ó Nego. ~ 11. 12. 25 ±îÁö 11-12-07 5087
311   Sr. Accountant 5³âÀÌ»ó Nego. ~ 11. 11. 6 ±îÁö 11-10-25 5291
310   ÀÓ»ó Auditor ¸ðÁý 2³âÀÌ»ó Ndgo. ~ 11. 11. 6 ±îÁö 11-10-12 5404
309   Product Manager(º´,ÀÇ¿ø Á¦Ç°) 4³âÀÌ»ó Nego. ~ 11. 11. 20 ±îÁö 11-10-11 5089
308   Sr. Regulatory Specialist 3³âÀÌ»ó Nego. ~ 11. 9. 25 ±îÁö 11-09-14 5140
307   Product Manager(ÀǾàǰ) 5³âÀÌ»ó Nego. ~ 11. 9. 20 ±îÁö 11-09-09 5385
306   PV(pharmacovigillan specialist 1³âÀÌ»ó Nego. ~ 11. 9. 20 ±îÁö 11-09-09 5278

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