我们的客户正在寻找一位能够梳理并规划治疗板块的发展战略，制定中长期研发计划，确定技术研究方向、研发管线等工作的CSO

Perform site monitoring and management to ensure that clinical trial sites and data reported are strictly in accordance to study protocols, regulations, guidelines and requirements.

You will be responsible for benchwork research focused on molecular biology and ensure experiment execution and timeliness to drive towards business goals.

小分子肿瘤创新药方向临床运营总监

1. 根据公司新药产品开发战略，负责制订部门的建设规划；

2. 负责管理并实施mRNA产品相关分析方法及质量体系的开发与建立，及相关检测工作；

PMO项目管理

* Works with the Head of Clinical Operations to ensure that Clinical Research activities are conducted in accordance to ICH GCP, relevant international and local regulations, requirements and guidelines

As one of the three function leads in biometrics department, has full responsibility for statistical programming team and system buildup, support drug development across the organization by contributing to drug development strategies, providing solutions to trial reporting events, managing program and study programming deliverable time-lines, develop SOP(s), and play managerial and mentoring role for junior programmers.

The Manager/Sr. Manager (title will be based on experience) will be responsible for management of statistical programming activities and study related projects while also developing and implementing SAS programs to efficiently produce analyses. Exercise judgement within generally defined practices and policies in selecting methods and policies.

Lead clinical project management team to ensure quality, time and budget deliverables are met to the Sponsor's satisfaction, and projects are appropriately resourced and employees are trained and developed to meet project needs. Work with related leadership team in formulating effective strategic goals and objectives for designated region and assures operational alignment with senior management priorities.

1、 负责所有的工艺开发流程，包括上游工艺开发、下游工艺开发、制剂工艺开发

2、负责MSAT团队管理

支持临床试验数据管理过程的各个方面，从研究启动到数据锁定

支持制定研究的临床报告（CSR）活动

筛选及管理供应商

临床项目一二三期经验

• To provide supply chain solution support for clinical research strategies, including import and export, drug batch distribution, packaging, labeling, etc.
• Timely adjust and optimize the supply strategy and establish supply chain related supplier system, reasonably control procurement costs and ensure quality.

Be accountable for the planning, implementation, management and reporting of clinical trials, which may not only in China, but included overseas.

Lead the clinical studies are executed in conformance with Good Clinical Practices (GCP) and in accordance with the International Conference of Harmonization (ICH) guidelines.

Take responsibilities of CRO and vendor selection, collaboration, management and performance.

大型集团公司肿瘤肿瘤创新药背景的临床PM

You will be responsible for being a Service Manager- Medical Device that strategically managing the treatment solutions service operations as well as developing the Service strategy for the Business Unit.

• Establish the validation system of the new preparation production plant to meet the requirements of FDA standards.
• Train other members of the team.

You will be responsible for overseeing clinical oversight activities in SEA to ensure the quality of all clinical trials practised.

You will be overseeing R&D projects focused on NGS, ensuring the conduction of experiments and delivery of results are efficient, timely and align with company goals.