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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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ÃѰԽù°: 711 ÃÑÆäÀÌÁö: 24 ÇöÀçÆäÀÌÁö: 7
¹øÈ£ ¸ðÁýºÎºÐ °æ·Â ¿¬ºÀ ¸ðÁý±â°£ ÀÛ¼ºÀÏ Á¶È¸
531   QA Specialist 3³âÀÌ»ó Nego. ~ 13. 10. 15 ±îÁö 13-09-10 4620
530   Sr. Accountant 5³âÀÌ»ó Nego. ~ 13. 10. 4 ±îÁö 13-09-10 4642
529   Product Manager 5³âÀÌ»ó Nego. ~ 13. 9. 1±îÁö 13-08-19 4638
528   RA Specialist 3³âÀÌ»ó Nego. ~ 13. 10. 15 ±îÁö 13-08-02 5072
527   Sales Director 15³âÀÌ»ó Nego. ~ 13. 6. 9 ±îÁö 13-05-30 5599
526   OTC(Consumer) Product Manager 5³âÀÌ»ó Nego. ~ 13. 8. 15 ±îÁö 13-05-10 5494
525   Sales Rep. 3³âÀÌ»ó Nego. ~ 13. 5. 25 ±îÁö 13-05-08 5326
524   Product Manager 2³âÀÌ»ó Nego. ~ 13. 10. 15±îÁö 13-04-26 5514
523   QA(Quality Engineering) 2³âÀÌ»ó Nego. ~13. 5. 5 ±îÁö 13-04-22 4840
522   QA(Quality Manager) 2³âÀÌ»ó Nego. ~ 13. 5. 5 ±îÁö 13-04-22 5155
521   Integration Lead 7³âÀÌ»ó Nego. ~ 13. 3. 25 ±îÁö 13-03-08 4388
520   ¹ÙÀÌ¿ÀÃѰý ´ã´ç ÀÓ¿ø 15³âÀÌ»ó Nego. ~ 13. 6. 9±îÁö 13-03-06 5306
519   Sales Rep. 1³âÀÌ»ó Nego. ~ 13. 3. 20 ±îÁö 13-03-06 4519
518   Sales & Marketing Manager 8³âÀÌ»ó Nego. ~ 13. 3. 10 ±îÁö 13-02-22 4970
517   Treasury Manager 10³âÀÌ»ó Nego. ~ 13. 2. 28 ±îÁö 13-02-13 5125
516   Sales Rep. 1³âÀÌ»ó Nego. ~ 13. 2. 13 ±îÁö 13-02-07 4819
515   Clinical Data Management Speci 3³âÀÌ»ó Nego. ~ 13. 2. 20 ±îÁö 13-02-06 5021
514   ¿µ¾÷°ü¸® ´ã´ç 8³âÀÌ»ó Nego. ~13. 2.10 ±îÁö 13-01-21 4535
513   RA(Regulatory Affairs) special 3³âÀÌ»ó Nego. ~ 2013. 1. 31±îÁö 13-01-18 4751
512   Policy Manager 5³âÀÌ»ó Nego. ~ 2013. 2. 10 ±îÁö 13-01-18 5214
511   Regulatory Affairs(Çã°¡/µî·Ï) 3³âÀÌ»ó Nego. ~ 12. 10. 21 ±îÁö 12-10-05 5438
510   º¯È£»ç 1³âÀÌ»ó Nego. ~ 12. 10. 21 ±îÁö 12-10-05 5526
509   RA(Regulatory Affairs) ´ã´ç °£ºÎ 8³âÀÌ»ó Nego. ~ 12. 10. 21 ±îÁö 12-10-05 5379
508   ¸¶ÄÉÆÃ ÆÀÀå 10³âÀÌ»ó Nego. ~ 12. 10. 15 ±îÁö 12-09-21 5651
507   Clinical Project Manager 3³âÀÌ»ó Nego. ~ 12. 10. 21 ±îÁö 12-09-19 5665
506   Product Specialist 5³âÀÌ»ó Nego. ~ 12. 10. 10 ±îÁö 12-09-19 5653
505   ¾à»ç(QA.QC,»ý»ê°ü¸®) 5³âÀÌ»ó Nego. ~ 12. 9. 26 ±îÁö 12-09-12 5207
504   Sales Rep. 1³âÀÌ»ó Nego. ~ 12. 9. 21 ±îÁö 12-09-12 4569
503   ¿µ¾÷´ã´ç ÀÓ¿ø 15³âÀÌ»ó Nego. ~2012. 10. 06 12-09-06 5448
502   Credit Analyst 3³âÀÌ»ó Nego. ~12 .09 . 15 ±îÁö 12-09-05 5515

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