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 ¸ðÁýºÎ¹®  Clinical Project Manager
 ¸ðÁýÀοø  0¸í
 ¾÷¹«³»¿ë  * Clinical Project Manager(Global ÀÓ»óÆÀ ¼Ò¼Ó)
- 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. 3. 31±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 4970
334   Biostatistics & Data Managemen 10³âÀÌ»ó Nego. ~ 12. 5. 28 ±îÁö 12-05-11 4950
333   PV(pharmacovigilance) 4³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-05-11 5077
332   Finance Manager 10³âÀÌ»ó Nego. ~ 12. 5. 18 ±îÁö 12-05-07 4875
331   HR Manager 10³âÀÌ»ó Nego. ~ 12. 7. 20 ±îÁö 12-05-07 4892
330   ¿¬±¸¿ø ¸ðÁý 3³âÀÌ»ó Nego. ~12. 4. 30 ±îÁö 12-04-23 5000
329   HR Manager 7³âÀÌ»ó Nego. ~ 12. 4. 28 ±îÁö 12-04-16 4960
328   Clinical Project Manager 5³âÀÌ»ó Nego. ~ 12. 3. 31±îÁö 12-03-16 5032
327   Pharmacovigillance Specialist 3³âÀÌ»ó Nego. ~ 2012. 3. 24 ±îÁö 12-03-15 4941
326   QA Specialist 3³âÀÌ»ó Nego. ~ 12. 3. 24 ±îÁö 12-03-15 4827
325   Drug Product Manager 3³âÀÌ»ó Nego. ~ 12. 3. 20 ±îÁö 12-03-06 4799
324   Bioassay Scientist 3³âÀÌ»ó Nego. ~ 12. 3. 20 ±îÁö 12-03-06 5080
323   Product Manager 5³âÀÌ»ó Nego. ~12. 2. 18 ±îÁö 12-02-08 4794
322   (Sr) Business Research special 4³âÀÌ»ó Nego. ~12. 2. 14 ±îÁö 12-02-06 4890
321   Medical Science Liason Manager 8³âÀÌ»ó Nego. ~12. 1. 31 ±îÁö 12-01-16 5042
320   ÇØ¿Ü»ç¾÷ & ¶óÀ̼¾½Ì ´ã´ç ÀÓ¿ø 15³âÀÌ»ó Nego. ~12. 2. 15 ±îÁö 12-01-06 5000
319   CRA 2³âÀÌ»ó Nego. ~ 12. 1. 13 ±îÁö 11-12-30 4943
318   Çмú´ã´ç(½ÅÀÔ or °æ·Â) ½ÅÀÔ Nego. ~ 12. 1. 13 ±îÁö 11-12-30 4690
317   ½Å·Ú¼º º¸Áõ ´ã´çÀÚ(QAU) 2³âÀÌ»ó Nego. ~ 12. 1. 13 ±îÁö 11-12-30 4952
316   ¾à¹° ºÐ¼® ¿¬±¸¿ø/½ÅÀÔ ¹× °æ·Â 1³âÀÌ»ó Neg. ~ 12. 1. 13 ±îÁö 11-12-30 4987
315   Sr. Regulatory Affairs Special 7³âÀÌ»ó Nego. ~ 12. 2. 15 ±îÁö 11-12-20 4897
314   Clinical Project Manager 5³âÀÌ»ó Nego. ~ 12. 2. 15 ±îÁö 11-12-16 4979
313   Regulatory Affairs(Çã°¡/µî·Ï)-Á¦¾à,ÀÇ 3³âÀÌ»ó Nego. ~ 11. 12. 31±îÁö 11-12-08 5043
312   Planning & Admin. Manager 10³âÀÌ»ó Nego. ~ 11. 12. 25 ±îÁö 11-12-07 4964
311   Sr. Accountant 5³âÀÌ»ó Nego. ~ 11. 11. 6 ±îÁö 11-10-25 5152
310   ÀÓ»ó Auditor ¸ðÁý 2³âÀÌ»ó Ndgo. ~ 11. 11. 6 ±îÁö 11-10-12 5293
309   Product Manager(º´,ÀÇ¿ø Á¦Ç°) 4³âÀÌ»ó Nego. ~ 11. 11. 20 ±îÁö 11-10-11 4960
308   Sr. Regulatory Specialist 3³âÀÌ»ó Nego. ~ 11. 9. 25 ±îÁö 11-09-14 5026
307   Product Manager(ÀǾàÇ°) 5³âÀÌ»ó Nego. ~ 11. 9. 20 ±îÁö 11-09-09 5254
306   PV(pharmacovigillan specialist 1³âÀÌ»ó Nego. ~ 11. 9. 20 ±îÁö 11-09-09 5164

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