临床研究项目经理 - Shanghai

This position is responsible for managing clinical trials from start to finish. The successful candidate will oversee project implementation, ensure quality control, and meet budget and timeline requirements. · Manage clinical trials from setup to closeout. · Ensure all project a ...

The Clinical Project Manager oversees clinical trials procedures from start to finish. They ensure all project activities adhere to SOPs and applicable regulations. · Review meeting minutes · Assure projects are completed within budget and schedule · Determine cause of project ov ...

+Job summary · The position involves leading clinical projects at Thermo Fisher Scientific. The role requires strong project management skills, ability to communicate effectively with customers and team members. · +QualificationsBachelor's degree or equivalent required. · +Skills ...

The Clinical Trial Administrator (CTA) is responsible for performing a variety of research, database, and clerical duties of a complex and technical nature in support of multiple clinical trials. · This position also provides administrative support to clinical teams by reviewing ...

Responsible for relatively simple and small size clinical trials according to the line manager guiding and supporting. · Review the Project contract exhibit to identify staff necessary for the project team. · ...

This position is responsible for managing overall study timelines, budgets and quality targets. The Senior Clinical Program Manager will lead the China core study team; manages, facilitates and documents core study team meetings (e.g. meeting agendas & minutes, action logs and de ...

This position is responsible for managing relatively simple and small size clinical trials according to contract and scheme requirements. Ensures all project activities follow SOPs, regulatory requirements, work scope, and clients' needs. · Review the Project contract exhibit to ...

This position requires managing overall study timelines, budgets, and quality targets. · Accountable for building forecasting and managing the Clinical Trial Budget. · Leads the China core study team manages facilitates and documents core study team meetings. · ...

This position is responsible for managing overall study timelines, budgets and quality targets. Accountable for building, forecasting and managing the Clinical Trial Budget. · ...

The Clinical Project Manager will lead clinical projects and teams in the region. · To serve as the primary liaison and primary point of escalation for clinical activities and team issues. · Leading a team of Clinical Operations colleagues (CRAs). · ...

The job involves managing clinical trial documents, assisting in the implementation of clinical trials, and performing administrative tasks. The role requires a bachelor's degree in pharmacy/nursing or other life sciences and strong communication skills.Manage TMF/eTMF in accorda ...

This position is responsible for managing TMF/eTMF in accordance with applicable regulations and guidelines. · ...

This position is responsible for managing overall study timelines, budgets and quality targets. Accountable for building, forecasting and managing the Clinical Trial Budget. · Fosters optimal China study team health including formal team effectiveness assessments and action plann ...

The Project Manager is primarily responsible for the planning and management of all contracted responsibilities for assigned projects and to act as the primary contact between Novotech and its clients. The role involves determining project feasibility, guiding scope of work, revi ...

This job is for a Clinical Trial Manager responsible for the operational management of regional/local clinical trials. · Accountable for trial recruitment commitment and timelines. · Leads local/regional trial team in the capacity of R/OPU Clinical Trial Manager (CTM). · ...

The Clinical Trial Assistant plays a fundamental role in the successful execution of global clinical trials. · Typical duties will include supporting other members of the local study team, · collecting data required for regulatory submissions, · document tracking contracts financ ...

The position involves developing in vivo models to test article activity and performing characterization of mechanisms studies in these models. · Candidate must have Master or PhD degree in immunology, immuno-oncology, pharmacology or veterinary medicine with at least three years ...

该职位来源于猎聘,主要负责临床试验管理,包括指导和带领其他临床监察员进行日常试验监察等. · 熟悉药品注册管理办法、药品临床试验及GCP等相关法规 · 清晰的书面和口头表达能力,善于进行活跃而积极的沟通 · ...

负责临床试验项目管理 · 负责临床试验的质量控制 · 负责供应商的管理 · ...

该职位来源于猎聘 岗位负责临床试验项目管理、供应商管理、文档编写以及组织重要会议等任务。 · ...