Description
- Leading the local study teams (consisting of monitors and study administrators) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines
- Ensuring that study sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived
- Ensuring timely submissions of proper application / documents to Ethic Committee / Regulatory Authority.
- Close communication with global study teams and overall responsibility for study commitments, for timely delivery of data to required quality as agreed with global
- Creating and implementing alternative action plans proactively in order to reach the targeted patient numbers; monitoring the patience admission processes in coordination with the researchers; planning and taking the necessary precaution when required
- Ensuring the compliance of the clinical research process with ICH-GCP practices, the study protocol, AZ Global and Local Clinical SOP’s, and the Ministry of Health Clinical Research Regulations; being knowledgeable about these procedures and keeping abreast of any changes and revision
- Participating in system / process improvement projects within global and local task groups consisting of employees from different units
Why AstraZeneca?
A high performing team, we work hard to not just meet but go beyond the needs of patients and the wider healthcare industry We leverage our partnerships with external experts across the industry, to create and communicate evidence that changes medical practice. As a partner for many, we effectively communicate complex ideas whilst seeking to understand ever-changing needs and requirements. Our valuable contribution and scientific expertise is responsible for advancing our pipeline and accelerating our pathway to finding a cure.
Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you.
Where can I find out more?
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Date Posted
28-May-2025
Closing Date
29-Haz-2025