Summit Therapeutics

Responsible for drafting, reviewing, and negotiating clinical and corporate contracts to protect the company from risk and support business objectives. Collaborates with internal departments and external parties to ensure compliance with legal and regulatory guidelines.

The Senior Manager, Clinical Site Partner serves as the primary operational contact for clinical trial sites, overseeing site performance from feasibility through study closeout. They drive study start-up efficiency, ensure regulatory compliance, and act as a strategic partner to investigators to deliver high-quality clinical trial execution.

The Clinical Supplies Manager will be responsible for planning and executing operations for assigned clinical supply projects, supporting the ongoing development pipeline, and optimizing processes within the Clinical Supplies department. This role requires effective collaboration across various phases of clinical development and serving as a key supply chain expert for cross-functional teams.

The Senior Manager will support day-to-day regulatory activities for assigned projects, including preparing and compiling submissions for regulatory agencies and managing clinical study processes and timelines. Responsibilities also involve driving regulatory content and strategy for marketing authorization submissions and providing internal regulatory guidance on study team decisions.

This role involves serving as a Safety Physician within a biopharmaceutical oncology company focused on improving patient quality and duration of life. The position supports global Phase 3 clinical studies evaluating investigational therapies like ivonescimab in cancers such as NSCLC and CRC.