Job Title: Clinical Research Associate Job Location: China Job Overview: The CRA monitors investigational sites to ensure subject safety and provide quality data review and reporting in compliance with the Caidya and/or client Standard Operating Procedures (SOPs), Good
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Job Description Responsible for scheduling and conduct of pre-study visits, initiation visits, interim monitoring visits and close-out visits according to the Monitoring Plan. Ensures the HGRAC and IRB submission and approval. Ensures assigned sites are conducting
Job Overview: The Contracts Specialist II (CS II) works in collaboration with project teams and the Contracts Lead (CL) to perform key study start-up tasks related to site contracts in their country, or countries, of expertise.