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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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 ÀüÈ­¹øÈ£  02-597-1780
 ±âŸ»çÇ×  [Á¢¼ö¹æ¹ý] E-mail : jiko01@kohuman.com (À̸ÞÀÏ Á¢¼ö¸¸ °¡´É)
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395   ¿¬±¸¿ø 3³âÀÌ»ó Nego. ~ 14. 2. 26 ±îÁö 14-02-12 4378
394   Product Manager 2³âÀÌ»ó Nego. ~ 13. 2. 5±îÁö 14-01-29 4255
393   ȸ°è ´ã´çÀÚ 3³âÀÌ»ó Nego. ~ 14. 07.11 ±îÁö 14-01-15 4173
392   ¸¶ÄÉÆà ½ÇÀå 15³âÀÌ»ó Nego. ~ 14. 1. 25 ±îÁö 14-01-15 4263
391   °æ¿µÁö¿ø½ÇÀå 15³âÀÌ»ó Nego. ~ 14. 7. 31 ±îÁö 14-01-15 4224
390   Bio Áø´Ü °³¹ß ´ã´çÀÚ 3³âÀÌ»ó Nego. ~14. 3. 12 ±îÁö 14-01-15 4282
389   Àü·«±âȹ½ÇÀå 15³âÀÌ»ó Nego. ~ 13. 3. 21 ±îÁö 14-01-03 4004
388   Marketing Director 15³âÀÌ»ó Nego. ~ 13. 12. 25 ±îÁö 13-12-13 4250
387   Åë°è ºÐ¼® ´ã´ç ½ÅÀÔ - ~ 13. 12. 7 ±îÁö 13-11-22 4003
386   Clinical Data Management 8³âÀÌ»ó Nego. ~ 13. 11. 30 ±îÁö 13-11-15 4210
385   Clinical QA 8³âÀÌ»ó Nego. ~ 13. 11. 30 ±îÁö 13-11-15 4073
384   RA(Regulatory Affairs) ´ã´ç °£ºÎ 8³âÀÌ»ó Nego. ~ 13. 11. 30 ±îÁö 13-11-15 3963
383   Clinical Project Manager(ÀÓ»ó) 8³âÀÌ»ó Nego. ~13. 11. 30 ±îÁö 13-11-15 4028
382   Medical Doctor ½ÅÀÔ Nego. ~ 13. 11. 30 ±îÁö 13-10-28 4024
381   ÀÇ·á±â °³¹ß ´ã´ç 3³âÀÌ»ó Nego. ~ 13. 10. 6 ±îÁö 13-09-17 4106
380   ÀǾàÇ° °³¹ß ´ã´ç 3³âÀÌ»ó Nego. ~ 13. 10. 6 ±îÁö 13-09-17 4032
379   QA Specialist 3³âÀÌ»ó Nego. ~ 13. 10. 15 ±îÁö 13-09-10 4381
378   Sr. Accountant 5³âÀÌ»ó Nego. ~ 13. 10. 4 ±îÁö 13-09-10 4430
377   Product Manager 5³âÀÌ»ó Nego. ~ 13. 9. 1±îÁö 13-08-19 4422
376   RA Specialist 3³âÀÌ»ó Nego. ~ 13. 10. 15 ±îÁö 13-08-02 4873
375   Sales Director 15³âÀÌ»ó Nego. ~ 13. 6. 9 ±îÁö 13-05-30 5379
374   OTC(Consumer) Product Manager 5³âÀÌ»ó Nego. ~ 13. 8. 15 ±îÁö 13-05-10 5303
373   Sales Rep. 3³âÀÌ»ó Nego. ~ 13. 5. 25 ±îÁö 13-05-08 5122
372   Product Manager 2³âÀÌ»ó Nego. ~ 13. 10. 15±îÁö 13-04-26 5280
371   QA(Quality Engineering) 2³âÀÌ»ó Nego. ~13. 5. 5 ±îÁö 13-04-22 4621
370   QA(Quality Manager) 2³âÀÌ»ó Nego. ~ 13. 5. 5 ±îÁö 13-04-22 4960
369   ¹ÙÀÌ¿ÀÃÑ°ý ´ã´ç ÀÓ¿ø 15³âÀÌ»ó Nego. ~ 13. 6. 9±îÁö 13-03-06 5094
368   Sales & Marketing Manager 8³âÀÌ»ó Nego. ~ 13. 3. 10 ±îÁö 13-02-22 4729
367   Treasury Manager 10³âÀÌ»ó Nego. ~ 13. 2. 28 ±îÁö 13-02-13 4889
366   Clinical Data Management Speci 3³âÀÌ»ó Nego. ~ 13. 2. 20 ±îÁö 13-02-06 4811

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