The Global Development Scientist Director, Clinical Excellence and Innovation will report directly to the Head, Clinical Excellence and Innovation and is an important part of the Late Development Oncology (LDO) Clinical Excellence and Innovation (CEI) team. Our LDO CEI team is an innovative, entrepreneurial team shaping and conducting the LDO R&D mission in all matters relating to clinical excellence, including performance, knowledge sharing, external engagement, innovation, data technology, and digitalization.
Accountabilities include clinical support for the development and implementation of late phase AstraZeneca sponsored clinical strategies and drug development initiatives. You will provide clinical/scientific expert input, lead functional process improvements, and provide contributions to cross-asset or cross-tumor area working groups. You will act as a resource related to clinical excellence and innovation for oncology physicians, scientists, and study teams. There will be a heavy emphasis on innovation/technology and data with AI, automation, digital across multiple areas.
You will contribute collaboratively to LDO Clinical Development and broader cross-functional teams, to ensure clinical strategy is translated in the adoption of technology in oncology clinical trials. You will share responsibility with LDO Clinical Project Teams, Clinical Operations, and Digital in the planning, execution, scaling, and delivery of initiatives across assets and across tumor areas. You will maintain and expand current professional knowledge in innovation and technology as applied to patients with cancer and oncology clinical trials. You will mentor others, and participate or lead review as needed for new opportunities, depending on level of experience.
This position demands strong collaborative communication skills, including the ability to engage with and influence a diverse range of stakeholders both within and external to AstraZeneca. The individual will operate according to the highest ethical standards in compliance with internal SOPs, local regulations, laws and adhere to Good Clinical Practice (GCP) and regulatory requirements.
Essential for the role
Desirable for the role