Therapy Program Manager Jobs In Shanghai - 14 Job Positions Available

Job TitleSr. Product Manager Image Guided Therapy Job Description In this role, you have the opportunity to Are you looking for a highly visible position where you can play a key role in creating and driving a new

Responsibilities Manage staff in accordance with organizations policies and applicable regulations, including without limitation: planning, assigning, and directing work; managing performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems;

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.

Typical Accountabilities Responsible for establishing study and trial level V2V process. Establish cell therapy site qualification criteria and conduct technical on-site assessment. Responsible for developing V2V related study and trial documents, creating apheresis and product administration manuals

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.

Locations: Shanghai, China Categories: Clinical Trial Management Req ID: 12855 The Clinical Trial Manager (CTM) position performs as project lead for multiservice clinical trials (some global in scope). The position interacts with sponsors and manages the timeline

Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental

岗位职责 / Key Responsibilities 1.推进揭榜挂帅项目（技术端）/ Promote Open Innovation Project 从市场趋势、技术先进性、产业化可行性与公司战略的契合度建立并执行生命科学项目的系统评估框架 Develop and execute a systematic evaluation framework for life science projects (technological advancement, team capability, industrialization feasibility, market potential, and strategic fit). 筛选、评估优质标的企业/项目，推动纳入本土开放式创新（Open innovation）暨“揭榜挂帅”项目池并跟进全流程 Screen and

Locations: Shanghai, China Categories: Site Activation & Maintenance Req ID: 12991 Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager in Beijing or Shanghai to join our Clinical

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and

Senior Clinical Support Associate Flex The Senior Clinical Support Associate Flex provides in-house administrative support to the clinical project teams according to project requirements, ICH GCP guidelines, local or global regulatory requirements and Novotech or Sponsor

Responsibilities Performing site evaluation, initiation, monitoring and close-out visits, plus maintaining appropriate documentation according to a project-specific monitoring plan, ICH-GCP, and applicable regulations. Supporting the development of a subject recruitment plan. Establishing regular lines of communication