Summit Therapeutics

The Senior Analyst will assist with SEC reporting, including the preparation and tie-out of forms 10-K and 10-Q. Additionally, the role involves managing month-end close activities, recording clinical trial expenses, and supporting internal and external audits.

Lead the commercialization and launch of ivonescimab in the East Coast region by managing a team of oncology account managers. Execute national sales strategies and collaborate with cross-functional partners to achieve regional market share goals.

Lead the operational execution of Phase I–III oncology clinical trials across Europe, serving as the primary point of contact for clinical sites. Drive site selection, activation, and recruitment while ensuring high standards of performance and quality throughout the study lifecycle.

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.

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.