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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. 10. 21 ±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 5006
364   Regulatory Affairs(Çã°¡/µî·Ï) 3³âÀÌ»ó Nego. ~ 12. 10. 21 ±îÁö 12-10-05 5244
363   º¯È£»ç 1³âÀÌ»ó Nego. ~ 12. 10. 21 ±îÁö 12-10-05 5329
362   RA(Regulatory Affairs) ´ã´ç °£ºÎ 8³âÀÌ»ó Nego. ~ 12. 10. 21 ±îÁö 12-10-05 5201
361   ¸¶ÄÉÆà ÆÀÀå 10³âÀÌ»ó Nego. ~ 12. 10. 15 ±îÁö 12-09-21 5427
360   Clinical Project Manager 3³âÀÌ»ó Nego. ~ 12. 10. 21 ±îÁö 12-09-19 5426
359   Product Specialist 5³âÀÌ»ó Nego. ~ 12. 10. 10 ±îÁö 12-09-19 5439
358   ¾à»ç(QA.QC,»ý»ê°ü¸®) 5³âÀÌ»ó Nego. ~ 12. 9. 26 ±îÁö 12-09-12 4996
357   ¿µ¾÷´ã´ç ÀÓ¿ø 15³âÀÌ»ó Nego. ~2012. 10. 06 12-09-06 5228
356   Credit Analyst 3³âÀÌ»ó Nego. ~12 .09 . 15 ±îÁö 12-09-05 5253
355   Product Manager 3³âÀÌ»ó Nego. ~ 12. 9. 21 ±îÁö 12-09-04 5130
354   ÇØ¿Ü ¿µ¾÷ ´ã´ç(ÀϺ») 5³âÀÌ»ó Nego. ~ 12. 9. 21 ±îÁö 12-09-04 4977
353   CRA /Clinical Research Associa 1³âÀÌ»ó Nego. ~ 12. 9. 14 ±îÁö 12-08-31 5160
352   Clinical QA 1³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-08-01 5236
351   Clinical Project Manager 4³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-07-26 5527
350   Local Project Manager 4³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-07-26 5050
349   HR Ã¥ÀÓÀÚ 10³âÀÌ»ó Nego. ~ 12. 8. 15 ±îÁö 12-07-26 5316
348   °øÀÎȸ°è»ç 4³âÀÌ»ó Nego. ~ 12. 8 . 19 ±îÁö 12-07-17 5309
347   Ç°Áú°ü¸® 1³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-07-12 5084
346   ÀÓ»ó°³¹ß 2³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-07-12 4878
345   RA ¹× °³¹ß¾÷¹« ´ã´ç 2³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-07-12 4904
344   CRA 1³âÀÌ»ó Nego. ~ 12. 8 . 19 ±îÁö 12-07-12 5000
343   Financial Planning Analyst 3³âÀÌ»ó Nego. ~ 12. 7. 13 ±îÁö 12-06-25 5029
342   Medical Doctor ½ÅÀÔ Nego. ~ 12. 8. 19 ±îÁö 12-06-20 5130
341   QA & RA Manager 10³âÀÌ»ó Nego. ~ 12. 6. 29 ±îÁö 12-06-15 4950
340   IT specialist 5³âÀÌ»ó Nego. ~ 12. 6 29 ±îÁö 12-06-11 5074
339   º¯¸®»ç 1³âÀÌ»ó Nego. ~ 12. 6. 29 ±îÁö 12-05-23 5203
338   º¯È£»ç 1³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-05-23 4874
337   Clinical Project Manager(ÀÓ»ó) 10³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-05-14 4931
336   Researcher(Ã¥ÀÓ/¼±ÀÓ ¿¬±¸¿ø) 2³âÀÌ»ó Nego. ~ 12. 5. 28 ±îÁö 12-05-11 4843

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