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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 5046
334   Biostatistics & Data Managemen 10³âÀÌ»ó Nego. ~ 12. 5. 28 ±îÁö 12-05-11 5036
333   PV(pharmacovigilance) 4³âÀÌ»ó Nego. ~ 12. 8. 19 ±îÁö 12-05-11 5167
332   Finance Manager 10³âÀÌ»ó Nego. ~ 12. 5. 18 ±îÁö 12-05-07 4949
331   HR Manager 10³âÀÌ»ó Nego. ~ 12. 7. 20 ±îÁö 12-05-07 4980
330   ¿¬±¸¿ø ¸ðÁý 3³âÀÌ»ó Nego. ~12. 4. 30 ±îÁö 12-04-23 5069
329   HR Manager 7³âÀÌ»ó Nego. ~ 12. 4. 28 ±îÁö 12-04-16 5035
328   Clinical Project Manager 5³âÀÌ»ó Nego. ~ 12. 3. 31±îÁö 12-03-16 5134
327   Pharmacovigillance Specialist 3³âÀÌ»ó Nego. ~ 2012. 3. 24 ±îÁö 12-03-15 5032
326   QA Specialist 3³âÀÌ»ó Nego. ~ 12. 3. 24 ±îÁö 12-03-15 4913
325   Drug Product Manager 3³âÀÌ»ó Nego. ~ 12. 3. 20 ±îÁö 12-03-06 4878
324   Bioassay Scientist 3³âÀÌ»ó Nego. ~ 12. 3. 20 ±îÁö 12-03-06 5158
323   Product Manager 5³âÀÌ»ó Nego. ~12. 2. 18 ±îÁö 12-02-08 4860
322   (Sr) Business Research special 4³âÀÌ»ó Nego. ~12. 2. 14 ±îÁö 12-02-06 4964
321   Medical Science Liason Manager 8³âÀÌ»ó Nego. ~12. 1. 31 ±îÁö 12-01-16 5124
320   ÇØ¿Ü»ç¾÷ & ¶óÀ̼¾½Ì ´ã´ç ÀÓ¿ø 15³âÀÌ»ó Nego. ~12. 2. 15 ±îÁö 12-01-06 5065
319   CRA 2³âÀÌ»ó Nego. ~ 12. 1. 13 ±îÁö 11-12-30 5014
318   Çмú´ã´ç(½ÅÀÔ or °æ·Â) ½ÅÀÔ Nego. ~ 12. 1. 13 ±îÁö 11-12-30 4762
317   ½Å·Ú¼º º¸Áõ ´ã´çÀÚ(QAU) 2³âÀÌ»ó Nego. ~ 12. 1. 13 ±îÁö 11-12-30 5020
316   ¾à¹° ºÐ¼® ¿¬±¸¿ø/½ÅÀÔ ¹× °æ·Â 1³âÀÌ»ó Neg. ~ 12. 1. 13 ±îÁö 11-12-30 5055
315   Sr. Regulatory Affairs Special 7³âÀÌ»ó Nego. ~ 12. 2. 15 ±îÁö 11-12-20 4976
314   Clinical Project Manager 5³âÀÌ»ó Nego. ~ 12. 2. 15 ±îÁö 11-12-16 5048
313   Regulatory Affairs(Çã°¡/µî·Ï)-Á¦¾à,ÀÇ 3³âÀÌ»ó Nego. ~ 11. 12. 31±îÁö 11-12-08 5109
312   Planning & Admin. Manager 10³âÀÌ»ó Nego. ~ 11. 12. 25 ±îÁö 11-12-07 5030
311   Sr. Accountant 5³âÀÌ»ó Nego. ~ 11. 11. 6 ±îÁö 11-10-25 5230
310   ÀÓ»ó Auditor ¸ðÁý 2³âÀÌ»ó Ndgo. ~ 11. 11. 6 ±îÁö 11-10-12 5355
309   Product Manager(º´,ÀÇ¿ø Á¦Ç°) 4³âÀÌ»ó Nego. ~ 11. 11. 20 ±îÁö 11-10-11 5035
308   Sr. Regulatory Specialist 3³âÀÌ»ó Nego. ~ 11. 9. 25 ±îÁö 11-09-14 5094
307   Product Manager(ÀǾàǰ) 5³âÀÌ»ó Nego. ~ 11. 9. 20 ±îÁö 11-09-09 5331
306   PV(pharmacovigillan specialist 1³âÀÌ»ó Nego. ~ 11. 9. 20 ±îÁö 11-09-09 5229

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