Clinical Research Project Coordinator  -Temporary  (1 year)

At AstraZeneca we win through science, it’s at the heart of our every success. That science is only possible when we all work together – we’ll always make sure you’re clear about how your role is connected to our wider mission to really show what science can do.

If you are relentlessly curious about science and, like us, believe that when we follow the science we can make game-changing discoveries that can transform the lives of patients around the world, we have an opportunity for you.

We are looking for a Clinical Research Project Coordinator to join our Evidence Generation Department, that comprises of two main areas: Real World Evidence and Clinical Trials.  

Responsibilities:

The role of the Clinical Research Project Coordinator is to support several ongoing and upcoming studies.

The position will monitor patient recruitment, enrollment, data and study-related information related to clinical study sites and study participation.

Oversight of service providers (eg .CROs) to ensure the service delivery is in line with the agreed time, cost and quality.

Education, Qualifications, Skills and Experience:

• Bachelor’s degree in relevant discipline
• Experience in clinical research - study implementation and management (at least 2-3 years)
• Proficiency in English, both written and oral

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.