• 电话: +86 21 63862192
  • 邮箱: info@alphabiopharma.com
  • 上海: 黄浦区太仓路233号新茂大厦504-508室
  • 北京: 朝阳区光华路9号世贸商业中心4号楼天阶大厦2512室

人才理念

组织能力指的是团队整体发挥的战斗力

  • 深植于组织内部
而非个人,有可持续性

    深植于组织内部
    而非个人,有可持续性

  • 为客户创造价值

    为客户创造价值

  • 明显超越竞争对手

    明显超越竞争对手

组织能力要聚焦,优秀的公司往往在两三个方面展示出众所周知的组织能力;组织能力还要清晰界定,这样团队才能集中精力和资源来关注、开发这样的能力。

  • 员工思维

    员工思维

    员工是否展现与组织能力匹配的价值观、 行为和投入度?

  • 员工能力

    员工能力

    员工是否具备组织能力行为和投入度?

  • 员工治理

    员工治理

    公司是否提供有效的管理支持和资源容许员工充分发挥所长?

打造组织能力的三个维度

打造组织能力的三个维度,必须符合两个原则:
一是平衡,即三个能力要一样强;
二是匹配,三个支柱的重点必须与所需的组织能力协调。
打造组织能力的三个维度

员工风采

icon
icon
ICON

icon
icon

员工发展与培训

  • 新员工培训

    新员工培训
  • 通用管理技能培训

    通用管理技能培训
  • 专业技能培训

    专业技能培训

培训方式

  • 现场培训现场培训
  • 在线直播课程在线直播课程
  • 午餐分享会午餐分享会
  • 线下培训沙龙
线下培训沙龙

员工福利

  • 福利年假
    福利年假
  • 带薪病假
    带薪病假
  • 商业保险
    商业保险
  • 年度旅游
    年度旅游
  • 年度体检
    年度体检
  • 生日会
    生日会
  • 下午茶
    下午茶
  • 节日福利
    节日福利
  • 团队建设
    团队建设
  • 员工班车#
    员工班车
  • 员工住宿#
    员工住宿
  • 福利午餐#
    福利午餐

出现icon为工厂员工专享福利

icon

招聘信息

QC流式细胞分析主管

  • 工作地点:上海
  • 发布时间:2021-06-24
  • 招聘人数:1人
点击收起

岗位描述

负责QC仪器/分析方法相关文件起草、审核;负责流式相关样本检测分析;协助QC负责人进行团队搭建及实验室的建设;确保实验室合规运行。

任职要求

工作内容:
1. QC 文件
负责相关仪器/方法的 SOP 起草,审核。
2. 分析方法建立,样本检测
1)负责按照 SOP 完成血样、细胞中间产品、细胞成品及稳定性留样等多种类型样本日常检测分析工作及
相关方法确认/验证工作执行;
2)熟练掌握和使用流式细胞仪及其分析软件,具备较强的上机操作能力及数据分析与处理能力;
3)按照要求完成流式检测样本实验记录和报告及时填写;
3. 仪器维护:负责流式分析仪器的日常清洁和维护;新人操作技能培训;
4. GMP 质量事件:参于实验室偏差/OOS/OOT/异常数据调查。

任职要求:
1. 具有二年以上流式操作经验;精通流式分析方法原理,熟练应用流式分析软件处理数据;
2. 有 GMP 工作经验者优先;
3. 具有数据分析、异常结果原因分析的能力,可以被培训并能够和其他部门同事共同合作。
4. 具有在 QC 团队高效工作的能力。良好的写作、团队合作及沟通技巧。
5. 良好的英语和中文沟通能力,能流利地说、写、读这两种语言。
6. 细胞生物学,临床检验学或相关专业本科以上。
上传简历
文件大小不超过3mb

临床研究助理

  • 工作地点:上海-浦东新区
  • 发布时间:2021-05-27
  • 招聘人数:1人
点击收起

岗位描述

Assist on arranging all kinds of meetings of department and recording meeting minutes. Assist on searching trial related medical literatures. Assist project manager and team in conducting all kinds of tasks. Assist project manager in designing project documents and form according to projects need Provide general administrative support to the Clinical Operations Department Assist study documents collecting, printing copyingstamp and mail according to the requirements of project managersCRAs. Assist on clinical trial related contracts signingtrackingcoding and filing. Update the status of clinical trial subjects on smartsheet per week. Update curative effect assessment of clinical trials on smartsheet per month. Update the clinical trial and site information as necessary.

任职要求

At least 1 years experience on CTA Familiar with GCP guidelines Be good at operating MS Office as well as use of database Knowledge of drug development process Knowledge of clinical trial methodology
上传简历
文件大小不超过3mb

生物统计负责人

  • 工作地点:Shanghai
  • 发布时间:2021-05-08
  • 招聘人数:1人
点击收起

岗位描述

This role provides statistical services including analysis, interpretation, design, and reporting or communication of data evidence for research, development, and/or product needs at Alpha Biopharma.

Demonstrates advanced data analytic expertise based on a foundation of statistical principles and a track record of applied experience
Be effective in the use of relevant computational tools for study, experiment, or trial research objectives.
Applies high quality statistical methodology in assigned projects with demonstrated understanding of the disease/scientific/functional area and health authority acceptability
Ensures application of appropriate statistical methods and generation of accurate and reproducible results working independently or by providing specifications to statistical programming colleagues. Produces clear, concise, well-organized, and error-free computer programs and statistical reporting content.
Provides critical input to the statistical lead or team in optimizing study or trial designs in line with study or trial objectives, and supports scenario simulations and sample size calculations based on relevant technical and disease/scientific/functional area knowledge.
Acquires and demonstrates knowledge in pharmaceutical research and development strategies and execution. Assists in providing experimental design, modeling, analysis planning, analysis execution, interpretation, and statistical communications support.
Complies with organization and company standard operating procedures in timely fashion, such as training and project time accounting. Understands and aligns with relevant regulatory guidances.
Contributes high quality and timely deliverables as assessed by stakeholders such as the project team, the clinical Operation team, and Sr. VP, Medical.
Ensures that documents, specifications, programs, and macros are consistent and comply with project and company standards. Follows best practices for Data Integrity.
Oversee the quality of data management if it is outsourced.
Demonstrates full proficiency in systems as well as a working knowledge of other relevant computational tools as required.
Participates as a member of professional organizations, such as attending meetings sponsored by professional organizations.

任职要求

Ph.D. in Statistics or related field with 5-10 years relevant experience, or Master’s in Statistics or related field with commensurate years of relevant experience.
Experience in data analysis and reporting in NDA filing
上传简历
文件大小不超过3mb