上海康德保瑞医学临床研究有限公司（武汉）招聘信息分享：
工作地点武汉，有意应聘者可电话咨询027-65390225，或发送简历到zhou_chenchen@wuxiapptec.com

临床程序员-2人
岗位职责：
同统计专家一起编写并审核临床统计计划书。
建立数据库；协同并监查数据录入
编写统计运算程序, 即SAS程序
为最终报告生成分析数据集和TFL（表格、图表和列表）
运行统计程序，帮助数据管理人员编写数据质量审查
使用并优化公司的SAS宏命令
与统计专家出具统计报告,对统计报告进行审核并提出具体意见。

任职要求：
大学本科及以上学历，数学、生物统计、临床卫生与流行病学相关专业。
能熟练运用SAS软件进行临床程序的编写和统计预算。

CRA Level 2
岗位职责：
1.Implements and monitors local/global clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH‐GCP guidelines
2.Manage the essential documents, as required by local regulations and ICH GCP, before, during and after a clinical trial, facilitates audit s and audit resolution
3. Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and close clinical trials at investigative sites
4. Reviews and verifies accuracy of clinical trial data collected, either onsite or remotely
5. Provides regular site status information to team members, trial management, and updates trial management tools
6. Completes monitoring activity documents as required by Company or Sponsor SOPs or other contractual obligations
7. Works closely with other clinical team members to facilitate timely esolution of trial and/or clinical issues

任职要求：
1.Undergraduate degree or its international equivalent in clinical, science, or health‐related field from an accredited institution; a licensed health‐care professional (i.e., registered nurse); or equivalent work experience required
2.2 to 4 years of local trial experience; exposure to MNC and global trials
3.Knowledge of ICH and local regulatory authority regulations regarding drug