Summit Therapeutics

Act as a field-based scientific expert to support oncology therapeutic areas and maintain relationships with healthcare professionals. Develop territory plans and support clinical research initiatives, including site evaluation and investigator-sponsored trials.

Oversee global Phase 3 clinical trials and BLA filings, focusing on protocol design and medical oversight. Lead cross-functional teams to execute clinical development goals and manage investigator engagements.

Lead global regulatory strategies to secure IND/CTA approvals and manage the planning and execution of global marketing applications (BLA/MAA) for oncology products. Act as the primary regulatory lead for development collaborations, partnerships, and cross-functional alignment across clinical and commercial teams.

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 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.