Sr. Clinical Research Associate

• Be responsible for initiating, organizing and managing the assigned studies.
• On site monitoring and site managements for global studies.
• Ensure clinical trials conducted in compliance with protocol & GCP.
• Ensure clinical trials can be conducted per timeline requirement.

Date Posted

Closing Date

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.