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Clinical Trial Project Manager ÁÙ´²ÊÔÑéÏîÄ¿¾Àí | [²é¿´¸ü¶àÀàËÆÖ°Î»] |
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¡¡2008-06-29 |
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ְλÀà±ð£º ÉúÎï/ÖÆÒ©/Ò½ÁÆÆ÷е ¹¤×÷µØµã£º ÉϺ£ ·¢²¼ÈÕÆÚ£º 2008-03-11 ¹¤×÷¾Ñ飺 ²»ÏÞ ×îµÍѧÀú£º ±¾¿Æ ¹ÜÀí¾Ñ飺 ·ñ ¹¤×÷ÐÔÖÊ£º ȫְ ÕÐÆ¸ÈËÊý£º Èô¸É ְλÃèÊö/ÒªÇó£º Responsibilities £º - Full project management responsibility - To initiate, monitor and close clinical trials in compliance with study protocol, GCP and SOP - To manage/resolve study related issues at sites independently - To develop and maintain good and effective communication with clinical research staff - Supervise junior CRAs Requirements: - University qualification in pharmacology/pharmacy, healthcare, medicine, biotech or related - At least 3 years of experience of conducting global clinical trials - At least 1 year project leader&management experience - Demonstrated knowledge and competence in, application of GCP and ICH guidelines - Very good written and spoken ability both in English (skills at IELTS 7.0 or above, or equivalent) and Chinese - Excellent Communication skills - Love serving clients and traveling - Result-oriented and can work under pressure - Good team player - Leadership quality ÁªÏµ·½Ê½£º .
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