A Clinical Research Associate (CRA) is a profession defined by Good clinical practice guidelines (ICH GCP). The main function of a clinical research associate is to monitor clinical trials. He or she may work directly with the sponsor company of a clinical trial, as an independent freelancer or for a Contract Research Organization (CRO). 一个 阅读更多
审计员, GCP Responsibilities The GCP Auditor is responsible for quality assurance auditing of all activities subject to the, “ICH 良好临床实践: 综合指南,” (地面控制点), 支持质量保证计划 (质量保证) to ensure that AGN project data and summary statements are of known and documented quality. Summary of Responsibilities: 阅读更多
要求: CRA (Freelance) JOB SUMMARY Our client requires a CRA for a 12 month contract position. You will be working on ophthalmology study. This role is field (home based) and applicants will need to have extensive monitoring experience. Competitive rates. JOB TITLE CRA/Clinical Research Associate/Freelance/Contract LOCATION Field Based/Home Based BENEFITS 阅读更多