New CRA opening at top global CRO company in Beijing, mature training process and system support your growth.
Your new company
As top global CRO, is recruiting for Clinical Research Associates to join their Clinical Monitoring department.
Your new role Monitors investigator sites to ensure the accuracy and validity of CRF entries in relation to patient records/clinic notes (source document verification).
Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards.
Escalates observed deficiencies and issues to clinical management expeditiously, present potential solutions and follow all issues through to resolution.
What you'll need to succeed
Proven clinical monitoring skills
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Demonstrated ability to attain and maintain a working knowledge of GCPs and applicable SOPs
What you'll get in return
Solid clinical trial experience with multiple therapeutic area under mature internal process and system.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. #1216148
Talk to a consultant
Talk to Olivia Huo, the specialist consultant managing this position, located in Beijing
501, Tower 1, China Central Plaza, 81 Jianguo Road, Chaoyang District