登录/注册我是招聘方 免费发布职位
CTMo Line Manager
35-65K/月北京市-北京/本科及以上/10年以上
赵女士一周前来过
百时美施贵宝（中国）投资有限公司
职位详情
Key Responsibilities and Major Duties
Supervises and coordinates the work assignments and performance of Clinical Operations staff inclusive of Clinical Trial Monitors (CTMs) to ensure timely execution consistent with R&D and local research goals and priorities
Demonstrates the ability to effectively communicate with and influence individuals at all levels of the organization including situations of conflict resolution, problem solving and crisis management.
Anticipates resource needs and provides workload evaluations and task assignments
Allocates and assign study resources in alignment with R&D and local research goals and priorities.
Supervises clinical trial execution at country level including supervising study metrics, KPI and team performance
Approves study fee funds and payments based on grant of authority
May propose and/or validate country study targets
May support Health Authority inspection and pre-inspection activities
May support audit preparation & Corrective Action / Preventative Action preparation for local related issues
Develops goals that are consistent with R&D and local research goals and priorities and takes necessary actions to ensure that goals are met
Together with the RCO management tracks and manages performance metrics for Clinical Operations staff
Anticipates and initiates action in response to multiple/changing demands and project priorities placed on Clinical Operations Unit
Point of Contact for FSP staff within the country
Managing the hiring, performance management and succession planning of staff
Performing general and human resource administrative functions
Participation in performance calibration and talent review meetings
Ensuring collaboration and information sharing with local country cross functional stakeholders (Medical, GRS, GPV, Market Access, Commercial, Human Resources)
Lead and contribute non study initiatives to optimized process and improve site management operation efficiency and productive.
When managing all RCO staff in a given country, will represent RCO in local leadership discussions at the affiliate level and may be member of the local affiliate leadership team managed by the General Manager
Ensure effective external partnerships with Study Sites, Investigators, Pharma Trade Associations, Ministry of Health and /or Heath Authorities as needed
Manage partnerships with critical accounts / sites
Supervises and coordinates the work assignments and performance of Clinical Operations staff inclusive of Clinical Trial Monitors (CTMs) to ensure timely execution consistent with R&D and local research goals and priorities
Demonstrates the ability to effectively communicate with and influence individuals at all levels of the organization including situations of conflict resolution, problem solving and crisis management.
Anticipates resource needs and provides workload evaluations and task assignments
Allocates and assign study resources in alignment with R&D and local research goals and priorities.
Supervises clinical trial execution at country level including supervising study metrics, KPI and team performance
Approves study fee funds and payments based on grant of authority
May propose and/or validate country study targets
May support Health Authority inspection and pre-inspection activities
May support audit preparation & Corrective Action / Preventative Action preparation for local related issues
Develops goals that are consistent with R&D and local research goals and priorities and takes necessary actions to ensure that goals are met
Together with the RCO management tracks and manages performance metrics for Clinical Operations staff
Anticipates and initiates action in response to multiple/changing demands and project priorities placed on Clinical Operations Unit
Point of Contact for FSP staff within the country
Managing the hiring, performance management and succession planning of staff
Performing general and human resource administrative functions
Participation in performance calibration and talent review meetings
Ensuring collaboration and information sharing with local country cross functional stakeholders (Medical, GRS, GPV, Market Access, Commercial, Human Resources)
Lead and contribute non study initiatives to optimized process and improve site management operation efficiency and productive.
When managing all RCO staff in a given country, will represent RCO in local leadership discussions at the affiliate level and may be member of the local affiliate leadership team managed by the General Manager
Ensure effective external partnerships with Study Sites, Investigators, Pharma Trade Associations, Ministry of Health and /or Heath Authorities as needed
Manage partnerships with critical accounts / sites
任职要求
无
薪资结构
无
其他信息
职能类别：临床监查
职位性质：全职
招聘人数：1
工作地点：
- 1 北京市-北京
公司信息
百时美施贵宝（中国）投资有限公司
- 上海
- 100-499人
- 生物制药、临床医疗服务
- 外企
- 不需要融资
百时美施贵宝公司是一家从事医药及相关保健产品生产的全球性企业，它的使命是＂延长人类寿命，提高生活质量＂。目前的主要业务包括中美上海施贵宝制药有限公司（SASS），美赞臣（广州）有限公司和百时美施贵宝中国肿瘤药物部。在中国现有员工约1,500人，有40多个知名品牌的药品、营养品和医疗器械在中国市场推广。百时美施贵宝中国肿瘤药物部于1992年正式成立。这十年来，百时美施贵宝优秀的抗癌药物和公司在肿瘤治疗领域的国际领先地位已被中国的肿瘤专家和社会公众所认识。目前，近50位医、药专业的营销人员在全国各主要城市进行总公司产品的介绍和推广。关于公司的更多信息，请浏览网站。为了满足公司业务的快速增长，我们欢迎有才之士与我们一起共创未来。
