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An executive medical affairs leader will guide oncology strategy and clinical development, support client proposals and business growth, and provide scientific expertise to internal teams. The role can be based in the EMEA region and requires travel to China; relocation may be considered.

Coordinate country-level regulatory and ethical submissions supporting clinical trial site activation in Israel. Prepare and review submission documents, advise internal teams on local requirements, and maintain accurate study records and timelines.

Manage clinical operations and quality for low- to moderate-complexity clinical studies in Israel, ensuring compliant delivery within agreed timelines, quality standards, and budgets.