¿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 5037
334   Biostatistics & Data Managemen 10³âÀÌ»ó Nego. ~ 12. 5. 28 ±îÁö 12-05-11 5024
333   PV(pharmacovigilance) 4³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-05-11 5154
332   Finance Manager 10³âÀÌ»ó Nego. ~ 12. 5. 18 ±îÁö 12-05-07 4938
331   HR Manager 10³âÀÌ»ó Nego. ~ 12. 7. 20 ±îÁö 12-05-07 4964
330   ¿¬±¸¿ø ¸ðÁý 3³âÀÌ»ó Nego. ~12. 4. 30 ±îÁö 12-04-23 5057
329   HR Manager 7³âÀÌ»ó Nego. ~ 12. 4. 28 ±îÁö 12-04-16 5018
328   Clinical Project Manager 5³âÀÌ»ó Nego. ~ 12. 3. 31±îÁö 12-03-16 5116
327   Pharmacovigillance Specialist 3³âÀÌ»ó Nego. ~ 2012. 3. 24 ±îÁö 12-03-15 5016
326   QA Specialist 3³âÀÌ»ó Nego. ~ 12. 3. 24 ±îÁö 12-03-15 4899
325   Drug Product Manager 3³âÀÌ»ó Nego. ~ 12. 3. 20 ±îÁö 12-03-06 4867
324   Bioassay Scientist 3³âÀÌ»ó Nego. ~ 12. 3. 20 ±îÁö 12-03-06 5144
323   Product Manager 5³âÀÌ»ó Nego. ~12. 2. 18 ±îÁö 12-02-08 4845
322   (Sr) Business Research special 4³âÀÌ»ó Nego. ~12. 2. 14 ±îÁö 12-02-06 4952
321   Medical Science Liason Manager 8³âÀÌ»ó Nego. ~12. 1. 31 ±îÁö 12-01-16 5108
320   ÇØ¿Ü»ç¾÷ & ¶óÀ̼¾½Ì ´ã´ç ÀÓ¿ø 15³âÀÌ»ó Nego. ~12. 2. 15 ±îÁö 12-01-06 5053
319   CRA 2³âÀÌ»ó Nego. ~ 12. 1. 13 ±îÁö 11-12-30 5001
318   Çмú´ã´ç(½ÅÀÔ or °æ·Â) ½ÅÀÔ Nego. ~ 12. 1. 13 ±îÁö 11-12-30 4750
317   ½Å·Ú¼º º¸Áõ ´ã´çÀÚ(QAU) 2³âÀÌ»ó Nego. ~ 12. 1. 13 ±îÁö 11-12-30 5006
316   ¾à¹° ºÐ¼® ¿¬±¸¿ø/½ÅÀÔ ¹× °æ·Â 1³âÀÌ»ó Neg. ~ 12. 1. 13 ±îÁö 11-12-30 5045
315   Sr. Regulatory Affairs Special 7³âÀÌ»ó Nego. ~ 12. 2. 15 ±îÁö 11-12-20 4956
314   Clinical Project Manager 5³âÀÌ»ó Nego. ~ 12. 2. 15 ±îÁö 11-12-16 5037
313   Regulatory Affairs(Çã°¡/µî·Ï)-Á¦¾à,ÀÇ 3³âÀÌ»ó Nego. ~ 11. 12. 31±îÁö 11-12-08 5097
312   Planning & Admin. Manager 10³âÀÌ»ó Nego. ~ 11. 12. 25 ±îÁö 11-12-07 5018
311   Sr. Accountant 5³âÀÌ»ó Nego. ~ 11. 11. 6 ±îÁö 11-10-25 5219
310   ÀÓ»ó Auditor ¸ðÁý 2³âÀÌ»ó Ndgo. ~ 11. 11. 6 ±îÁö 11-10-12 5345
309   Product Manager(º´,ÀÇ¿ø Á¦Ç°) 4³âÀÌ»ó Nego. ~ 11. 11. 20 ±îÁö 11-10-11 5024
308   Sr. Regulatory Specialist 3³âÀÌ»ó Nego. ~ 11. 9. 25 ±îÁö 11-09-14 5083
307   Product Manager(ÀǾàǰ) 5³âÀÌ»ó Nego. ~ 11. 9. 20 ±îÁö 11-09-09 5318
306   PV(pharmacovigillan specialist 1³âÀÌ»ó Nego. ~ 11. 9. 20 ±îÁö 11-09-09 5217

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