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JOB Title : ±Û·Î¹ú Á¦¾à»ç CRA 2³âÀÌ»ó
Job Description
1) To manage and be responsible for all aspects of monitoring and site management for assigned R&D Clinical trials
2) To be responsible for assuring adequate control of investigational product
3) To be responsible for training the investigator and site staff on the regulatory guidelines/procedures for timely reporting and monitoring ongoing compliance to ensure overall patient safety
4) To be responsible for the preparation of site audits and regulatory inspections to ensure a successful outcome
5) Comply with pharmaceutical regulations and ethical business practices
Qualification
1) Major in Pharmacy, Nursing or Science preferred
2) 2 or 5 years of CRA experience in pharmaceutical industry preferred
3) Full knowledge of regulations
4) Capability of communicating clinical pharmacology
5) Good command of written and spoken English Reporting To CRM
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010-5397-7177
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jane@innohr.co.kr
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