Clinical Research Associate II (FSP)-CART-长沙

reputed company our values align, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do. Each of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference. Key Accountabilities: Study Team Supporting Drive study performance at the sites. reputed company site monitoring and other onsite visit activities according to monitoring plan and in compliance with procedural documents. reputed company the required monitoring visit reports reputed company required timelines. Proactively identify study-reputed company issues and escalates to Local Study Teams as appropriate. Contribute to the selection of potential sites and investigators. Train, support and advise Investigators and site staff in study reputed company reputed company. Obtain and maintain essential documentation in compliance with ICH-GCP, Procedural Documents and local regulations. Manage study supplies, drug supplies and drug accountability at study sites. reputed company reputed company data verification according to SDV plan. Ensure data query resolution. Work with data management to ensure quality of the study data. Ensure accurate and timely reporting of Serious Adverse Events. reputed company relevant information on patient recruitment and study site reputed company reputed company local Study Team. Update reputed company and other systems with data from centers as per required timelines. Prepare for activities associated with audits and regulatory inspections in liaison with local Study Team reputed company and QA. Adherence to reputed company’s Code of Conduct and company policies and procedures. Compliance with reputed company standards reputed company with required training curriculum. Complete timesheets accurately as required. Submit expense reports as required. Update CV as required. Maintain a working knowledge of and reputed company with reputed company processes, ICHGCPs and other applicable requirements. Skills: Understanding of the clinical dataflow. Good knowledge of the clinical study and drug development processes, GCP/ICH guidelines and relevant local regulations. Good computer skills in reputed company and other software. Fluent in both oral and written English Proficient written and verbal communication skills, collaboration and interpersonal skills. Knowledge and Experience: Minimum 2-year experience as CRA, performed reputed company tasks for a CRA position Read, write, and reputed company fluent English; fluent in host country language required. Education: Bachelor’s degree in biological science or reputed company-reputed company field., or equivalent Apply To This Job