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 ¸ðÁýºÎ¹®  Clinical Project Manager
 ¸ðÁýÀοø  0¸í
 ¾÷¹«³»¿ë  - Ensuring management of trials are done in compliance with ICH, GCP, company global standards,
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.
- Ensuring clinical trials are effectively executed and completed within budget, timelines and
meeting enrollment commitments as well as routine updating of CTMS and other clinical systems.
Pro-active trial management to identify challenges, develop effective mitigation plans and to
appropriately escalate and inform all relevant parties.
- 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 and to oversee appropriate final
disposition of IMP.
- Ensure clinical study site close-out in accordance with local regulations and ensure dissemination
of clinical trial results to the participating study investigators. Oversee appropriate file
archiving of all relevant study materials in accordance with local law and company guidelines.
 Áö¿øÀÚ°Ý - CRA 3³âÀÌ»ó °æ·Â
- Good Command of English
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 ¸ðÁý±â°£  ~ 12. 8. 19 ±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¦¾àȸ»ç

ÃѰԽù°: 515 ÃÑÆäÀÌÁö: 18 ÇöÀçÆäÀÌÁö: 6
¹øÈ£ ¸ðÁýºÎºÐ °æ·Â ¿¬ºÀ ¸ðÁý±â°£ ÀÛ¼ºÀÏ Á¶È¸
365   Policy Manager 5³âÀÌ»ó Nego. ~ 2013. 2. 10 ±îÁö 13-01-18 5180
364   Regulatory Affairs(Çã°¡/µî·Ï) 3³âÀÌ»ó Nego. ~ 12. 10. 21 ±îÁö 12-10-05 5408
363   º¯È£»ç 1³âÀÌ»ó Nego. ~ 12. 10. 21 ±îÁö 12-10-05 5488
362   RA(Regulatory Affairs) ´ã´ç °£ºÎ 8³âÀÌ»ó Nego. ~ 12. 10. 21 ±îÁö 12-10-05 5355
361   ¸¶ÄÉÆÃ ÆÀÀå 10³âÀÌ»ó Nego. ~ 12. 10. 15 ±îÁö 12-09-21 5620
360   Clinical Project Manager 3³âÀÌ»ó Nego. ~ 12. 10. 21 ±îÁö 12-09-19 5611
359   Product Specialist 5³âÀÌ»ó Nego. ~ 12. 10. 10 ±îÁö 12-09-19 5619
358   ¾à»ç(QA.QC,»ý»ê°ü¸®) 5³âÀÌ»ó Nego. ~ 12. 9. 26 ±îÁö 12-09-12 5174
357   ¿µ¾÷´ã´ç ÀÓ¿ø 15³âÀÌ»ó Nego. ~2012. 10. 06 12-09-06 5409
356   Credit Analyst 3³âÀÌ»ó Nego. ~12 .09 . 15 ±îÁö 12-09-05 5457
355   Product Manager 3³âÀÌ»ó Nego. ~ 12. 9. 21 ±îÁö 12-09-04 5322
354   ÇØ¿Ü ¿µ¾÷ ´ã´ç(ÀϺ») 5³âÀÌ»ó Nego. ~ 12. 9. 21 ±îÁö 12-09-04 5155
353   CRA /Clinical Research Associa 1³âÀÌ»ó Nego. ~ 12. 9. 14 ±îÁö 12-08-31 5336
352   Clinical QA 1³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-08-01 5420
351   Clinical Project Manager 4³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-07-26 5700
350   Local Project Manager 4³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-07-26 10191
349   HR Ã¥ÀÓÀÚ 10³âÀÌ»ó Nego. ~ 12. 8. 15 ±îÁö 12-07-26 5483
348   °øÀÎȸ°è»ç 4³âÀÌ»ó Nego. ~ 12. 8 . 19 ±îÁö 12-07-17 5483
347   ǰÁú°ü¸® 1³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-07-12 5255
346   ÀÓ»ó°³¹ß 2³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-07-12 5038
345   RA ¹× °³¹ß¾÷¹« ´ã´ç 2³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-07-12 5086
344   CRA 1³âÀÌ»ó Nego. ~ 12. 8 . 19 ±îÁö 12-07-12 5174
343   Financial Planning Analyst 3³âÀÌ»ó Nego. ~ 12. 7. 13 ±îÁö 12-06-25 5208
342   Medical Doctor ½ÅÀÔ Nego. ~ 12. 8. 19 ±îÁö 12-06-20 5298
341   QA & RA Manager 10³âÀÌ»ó Nego. ~ 12. 6. 29 ±îÁö 12-06-15 5159
340   IT specialist 5³âÀÌ»ó Nego. ~ 12. 6 29 ±îÁö 12-06-11 5230
339   º¯¸®»ç 1³âÀÌ»ó Nego. ~ 12. 6. 29 ±îÁö 12-05-23 5372
338   º¯È£»ç 1³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-05-23 5028
337   Clinical Project Manager(ÀÓ»ó) 10³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-05-14 5077
336   Researcher(Ã¥ÀÓ/¼±ÀÓ ¿¬±¸¿ø) 2³âÀÌ»ó Nego. ~ 12. 5. 28 ±îÁö 12-05-11 4994

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