Senior Clinical Research Associate
On-site · Beijing, Beijing, China
Job Summary
Senior Clinical Research Associate responsible for scheduling and conducting pre-study visits, initiation visits, interim monitoring visits and close-out visits according to the Monitoring Plan. Ensures IRB submission and approval. Verifies that sites conduct studies per protocol and regulations, protects rights and wellbeing of human subjects, and ensures accurate, verifiable data from source documents. Performs SDV against CRF/EDC, maintains Investigational Product accountability, and ensures site facilities remain adequate. Communicates deviations to investigators and project management, delivers quality reports, supports site audits and feasibility assessments, and may assist in monitoring guidelines/tools. 10% domestic travel. Full-time role. Have experience in multinational pharma, Medical Device trials; familiarity with QMS; strong English; path to bring clinical medicine/pharmacy background; added value for pathology background.
Required Qualifications
- Bachelor's or Master’s Degree or University Degree or equivalent
- At least 3 years CRA working experience in multinational pharmaceutical, Medical Device company or CRO
- Medical Device or IVD clinical trials experience
- Familiar with clinical trial Quality Management System
- Good English skills
- Willing to learn, hard working
- Major in clinical medicine or pharmacy; Pathology would be a plus
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.