[°ûÁöÇý] (homebase) CRA °æ·Â 3³âÀÌ»ó °æ·ÂÀÚ ¸ðÁý

Date 12/09/2010   Hits 1143

1. ÀÇ·Ú»ç: ¼¼°è ÃÖ´ë ±Û·Î¹ú CRO

2. ¸ðÁý ³»¿ë : (homebase) CRA °æ·Â 3³âÀÌ»ó °æ·ÂÀÚ ¸ðÁý

- University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).
- Minimum three (3) or more years of relevant clinical research experience in pharmaceutical or CRO industries.
- Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements.
- Ability to monitor study sites independently according to protocol monitoring guidelines, S.O.P.s, GCP and ICH Guidelines.
- Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.
- Fluent in local office language and in English, both written and verbal.
- Thorough knowledge of monitoring procedures.
- Basic understanding of the clinical trial process.
- homebase or office based. ¼±Åà °¡´É!

¢Ã ¿¬ºÀ¼öÁØ ¹× º¹¸®ÈÄ»ý: Çö, ¿¬ºÀ ÀÌ»ó ÃßÈÄ °æ·Â¿¡ µû¶ó ÇùÀÇ °¡´É / homebase or office based. ¼±Åà °¡´É!

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¢Ã ´ã´çÀÚ: °ûÁöÇý
¿¬¶ôó : 02-567-7407,7408
À̸ÞÀÏ : yskim@jhhr.co.kr