Job Description Support of the company Portfolio (85%) Lead cross-functional project teams in the strategy planning, execution, and delivery of China new product development projects. Develop project milestones and deliverables; prepare reports that summarize key progress
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical trials
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical trials
Job Overview: The Clinical Trial Manager I has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities
Main Accountabilities 主要职责 Ø Compliance · Developing, implementing, and maintaining an effective compliance program · Ensuring that the site complies with all laws, regulations, and standards applicable in the pharmaceutical industry · Maintaining a system to
Clinical Research Associate (CRA) Job Description The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP), and applicable Project Management Plan (PMP) and local
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical trials
At ABB, we help industries run leaner and cleaner—and every person here makes that happen. You’ll be empowered to lead, supported to grow, and proud of the impact we create together. Join us and help run
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
Job Description Role Summary: The EHS Manager is responsible for establishing and maintaining a safe, healthy, and environmentally compliant operating environment at the beverage manufacturing plant. This role leads the development and implementation of the EHS
Job Description: ACCOUNTABILITY Monitoring Policy / Compliance of Flight Training administration.(Pre-Requisite of Trainees; Flight Instructor Dossier; Competency updating; Issuing Flight Training Certificate, Course type updates, Process or Procedure updates, ATO Documents updates etc.) Support of the
The Clinician is accountable for the medical and scientific integrity of one or more clinical trials and for the safety and well-being of study participants. The role applies clinical and scientific expertise to design, execute, monitor,
Job Information 职位信息 Job title职位名称: QA Specialist QA专员 Location工作地点： Beijing, China 中国北京 % Remote working and % of travel expected 远程办公和出差的概率：N/A Job type工作类型: Full time全职 Site/Unit 区域/事业部：Beijing Site/ M&S China北京工厂/中国制造与供应事业部 About the job工作职责 Our Team我们的团队： The
Company Description Do you want beneficial technologies being shaped by your ideas? Whether in the areas of mobility solutions, consumer goods, industrial technology or energy and building technology - with us, you will have the chance