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| The Position |
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The role of the Clinical Research Associate (CRA) is the primary point of contact between investigational site
and Novo Nordisk. You will be responsible for taking leadership of site management for the selection and
initiation of sites as well as conduction and closing activities of the appointed studies in compliance with
local regulations, ICH-GCP, company procedures and protocol requirements to ensure date quality and study
subject protection.
You will be responsible for recruitment at country/ site level and thereby delivers results that have a direct
impact on the successful completion of the clinical programme. You coordinate with the Project Manager and
communicates to them progress and critical issues that may impair trial success.
You will be responsible for the recruitment at site level and communicate to the local trial manager for any
progress and/or issues that may in pair trial progress.
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| Qualifications |
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ㆍBachelor degree in Medicine, Pharmacy, Nursing, Life Sciences or equivalent is preferred
ㆍICH GCP trained and if applicable, certified
ㆍMinimum of five years of work experience as CRA
ㆍStrong leadership and good communication skill
ㆍPreferably, be fluent in written and spoken English
ㆍExcellent IT skill including MS Office package (word, Excel and Power point)
ㆍGood knowledge of ICH GCP, KGCP and other clinical research |
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| About the Department |
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The Clinical, Medical, Regulatory (CMR) department is one of the key functions that enable the business
strategy through effective execution of functional goals, in the areas of Clinical Research, Medical Affairs, and
Regulatory. The position Clinical Research Associate is to be located at Seoul South Korea, and report to the
Clinical Project Manager.
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