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Clinical Project Manager |
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- 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. |
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02-597-1780 |
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[Á¢¼ö¹æ¹ý] E-mail : jiko01@kohuman.com (À̸ÞÀÏ Á¢¼ö¸¸ °¡´É) |
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