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
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
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
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
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
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
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
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
About Human Pharmaceutical Business With global presence, Boehringer Ingelheim has industry-leading expertise in medicine research and development. We are constantly developing the next generation of medical breakthroughs and successfully delivering innovations to meet the medical needs
Company Description For more than 40 years, the IOTA Group has been supporting clients in their international expansion by combining compliance, agility, and seamless local integration across more than 150 countries. We provide tailored solutions that
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