上海法码康医药科技有限公司 |
| 来源：生物资讯网 作者：无 发布时间：2008-06-11 |
| Pharmacons is a professional pharmaceutical services provider comprising a group of experienced and enthusiastic professionals at all levels of management coming from global leading pharmaceutical and Contract Research Organization (CRO) companies.
Pharmacons has offices in Australia and China, and associates in America, Japan and other Asian countries to service clients' R&D needs in the region with international standard performance in various disciplines. Pharmacons has the systems and processes supported with our long term experience and the skills of our people in the region.
To facilitate the company's development in China and Asia Pacific Region, experienced and passionate CRAs and Bio-statisticians are welcomed to join this growing team.
Top salary packages will be offered to top candidates. Pharmacons provides you friendly and stimulating work environment and various long term career opportunities. 联系方式：
招聘：临床研究员－CRA－（全球性试验经验）
联系人:人事部 邮编:200052 地址:上海市淮海西路288号1号楼302B 工作地点：上海 招聘人数：若干名 学历要求：本科 工作年限：一年以上 薪水范围：面议 Responsibilities: - 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 Requirements:
- 1 years of experience or above on global Clinical trials is a must
- University qualification in pharmacology/pharmacy, healthcare, medicine, biotech or related - Demonstrated knowledge of, and competence in, application of GCP and ICH guidelines - Good written and spoken ability both in English (skills at IELTS 6.5 or above, or equivalent) and Chinese - Excellent Communication skills - Love serving clients and traveling - Result-oriented and can work under pressure - Good team player 招聘：Clinical Trial Project Manager 临床试验项目经理 联系人:人事部 邮编:200052 地址:上海市淮海西路288号1号楼302B 工作地点：上海 招聘人数：若干名 学历要求：本科 工作年限：一年以上 薪水范围：面议 Responsibilities： - 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 招聘：生物统计师（Bio-Statistician） 联系人:人事部 邮编:200052 地址:上海市淮海西路288号1号楼302B 工作地点：上海 招聘人数：若干名 学历要求：本科 工作年限：一年以上 薪水范围：面议 Responsibilities: - Offer statistical input to protocol design - Review protocol, Case Report Form (CRF) and Data Validation Plan (DVP) - Prepare Statistical Analysis Plan (SAP) - Prepare for and participate in database release meeting - SAS programming, statistical analyses and preparation of output according to SAP. - Review Clinical Trial Report, presentation slides and scientific publications for statistical and scientific contents - Ensure documentation for the trial in accordance to ICH GCP guidelines and SOPs Requirements:
- Bachelor degree in scientific or biomedical area, preferable major in statistics, master degree is desirable - 2 years of biostatistician, SAS programming experience, working experience in clinical studies is desirable - Data management experience preferred - Knowledge and experience in designing and planning clinical trials - High degree of skill in the resolution of SAS programming issues and sample size calculation softwares - Fluent in written and spoken English - Ability to plan and prioritize complex tasks and approach these in a flexible manner. - Ability to work effectively as a good team member |
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