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Associate Director, Gcs Business Technology Solutions
hace 3 meses
Associate Director, GCS Business Technology Solutions Job Title: Associate Director, GCS Business Technology Solutions
Introduction to Role:
Join us at AstraZeneca as an Associate Director in our GCS Business Technology Solutions team. This role is a key part of our Biopharma Clinical Operations, where you will be responsible for the leadership, lifecycle management, and continuous improvement of specific processes, systems, or services. You will work collaboratively with internal and external customers and stakeholders to ensure customer needs are met and to enable optimal end-to-end delivery of clinical studies. Be empowered to act fast on smart risks and keep ahead in the fast-paced Oncology field.
Accountabilities: As an Associate Director, you will be responsible for the design, development, implementation, maintenance, and continuous improvement of our systems. You will ensure compliance with industry regulations and AstraZeneca Global and Local Policies. You will provide training, advice, and end-user support. You will engage and influence internal and external key partners to drive the strategy, development, and continuous improvement of our systems. You will monitor performance, define key performance indicators, and use these data to inform selection of process improvements. You will also support audit and regulatory inspection planning, preparation, and conduct.
Minimum Requirements: Bachelor's of Science in an appropriate subject area or equivalent experience.
Extensive knowledge of Drug Development within a pharmaceutical or clinical background
High level of business process, technology and Clinical Study information experience
Demonstrated project management skills to deliver to time, cost and quality
Ability to collaborate with, motivate and empower others
Demonstrated excellent written, verbal and influencing skills
Experience in Medidata Rave including iMedidata user and site administration
Expert reputation within the business and industry
Experience of utilising standard process improvement methodologies (e.g. Lean Six Sigma)
Comprehensive knowledge of ICH/GCP
Extensive experience in Validation of computerised systems in a regulated environment
Medidata Study Builder certification
Experience in other EDC systems (e.g Veeva, Bioclinica)
Are you ready to push the boundaries of science to change the practice of medicine? Apply now to join us in our mission
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