[°ûÁöÇý] ¿ÜÀÚ, Study Authorisation Associate(Á¤±ÔÁ÷) ¸ðÁý

Date 07/19/2011   Hits 1149

1. ÀÇ·Ú»ç: ¿ÜÀÚ CRO

2. ¸ðÁý ³»¿ë : Study Authorisation Associate ¸ðÁý

¢Ã Position : Study Authorisation Associate ¸ðÁý (Á¤±ÔÁ÷)

- Working within a highly qualified team you will prepare submissions packages for the country specific Regulatory Authorities and Ethics Committees for the region within which you work. You will liaise with the authorities as appropriate regarding amendments and questions relating to start up activities.

- With a University degree in medicine, science, or equivalent, you will have previous submissions/dossier experience within clinical studies for either a CRO or Pharma company. In addition you will also require:

- Knowledge of ICH GCP guidelines and expertise to review and evaluate medical data

- Demonstrate an understanding of regionally specific legislation surrounding ethics committees and submissions procedures and practices

- Have excellent interpersonal and presentation skills and the ability to interact at all levels in this client facing role

- Bi-Lingual - you must be fluent native speaker with fluent English since all submission documents to sponsors and many authorities must be compiled in
English

- Ability to prioritize work, have excellent attention to detail, demonstrate a pro-active attitude and have previously worked within a team.

- Good working knowledge of Microsoft applications especially PowerPoint.


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