Assist with coordination the Clinical Data Management (CDM) deliverables on assigned clinical studies and may
be an expert on CDM processes, standards and technology. May be member of the Global Study Team (GST) for
less complex studies. Collaborates with DM vendors and liaise with a variety of departments on a local and/or
global level to ensure each study is run in accordance to the specifics of the model. Maintains Business
Continuity for CDM processes and standards including integrity of the clinical database for the relevant studies.
May work under direction of an experienced Principal Clinical Data Manager.

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.