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Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Senior Manager, Global Data Generation - **Company:** The Summit - **Location:** Palo Alto, CA, United States - **Experience:** Expert - **Salary:** $158,000.0 - $185,000.0 - **Contract:** Permanent contract - **Skills:** Microsoft Word, Microsoft Excel, Computing Platforms, Clinical Trial Management Systems, Document Management Systems, Microsoft Office, Microsoft PowerPoint, Data Delivery, Data Generation - **Published:** October 21, 2026 - **Apply:** https://www.indeed.com/viewjob?jk=c89a7b8950f037b7 ## About the Role * Bachelor's or master's degree in life sciences with relevant experience; an advanced degree (e.g., PharmD, PhD) is preferred * 3+ years of relevant experience working in clinical trial management in CRO, pharmaceuticals/biotech, or related roles within the pharmaceutical or healthcare industry * In-depth understanding of the healthcare and pharmaceutical landscape and phases of clinical drug development and processes, including regulatory requirements * Familiarity with software platforms for managing ISTs (e.g. iEnvision ISR platform) and tools and fair market value analysis (e.g. IQVIA Grant Plan for Investigators) * Scientific and medical terminology acumen, experience in Oncology strongly preferred * Strong organizational skills, attention to detail, critical thinking and high problem-solving abilities * Excellent communication and interpersonal abilities * Ability to work collaboratively across diverse teams and manage multiple stakeholders * Proficient user of the standard MS Office suite (e.g., Word, Excel, PowerPoint); experience with electronic document management systems and document review tools is desirable * Self-motivated, ability to multi-task and work independently and achieve success with little oversight or guidance ## Description Summit Therapeutics is seeking a Senior Manager, Global Data Generation (Sr. Mgr.), to join our mission of developing Ivonescimab, a novel and unique immunotherapy with the potential to help patients suffering from life-threatening cancers. This position will focus on supporting the Global Non-Sponsored Research Program led by Medical Affairs, including Investigator Sponsored Trials (ISTs), Cooperative Group studies, as well as real-world evidence studies. The Sr. Mgr. contributes to key aspects of the program and is responsible for activities associated with the activation, tracking, and reporting of study-related information. This role provides an opportunity to work in a cross-functional environment, interfaces frequently with Summit's Scientific Review Committee, field medical affairs, external collaboration partners and investigators, including key opinion leaders. The ideal candidate will thrive in a fast-paced environment and be adept at collaborating with external stakeholders and cross-functional internal teams. Role and Responsibilities: * Manage all operational aspects of studies, including protocol/consent review, document management, fair market value evaluations, contract execution, drug shipments, and maintain ongoing oversight of project to ensure timelines and team goals are met * Manage the concept proposal intake process, maintain the submission portal and review status, document decisions and communicate with investigators and research coordinators * Assist with agenda and prepare meeting materials/minutes for Scientific Review Committee meetings * Responsible for obtaining internal approval of associated study budget, perform Fair Market Value analysis, conduct budget negotiations when needed * Work closely with Regional Medical Science Directors (RMSDs)/Medical Science Liaisons (MSLs), principal investigators, and other external parties to maintain central progress tracker for all approved proposals to ensure study timelines are met * Support ongoing analyses, tracking and reporting of study progress versus timelines committed by investigators, data delivery and program impact, and other related metrics * Track achievement of milestones that trigger payment, and work with Finance to perform budget reconciliation as well as forecast future milestones * Work with study site/drug supply team to manage and forecast drug supply for the program * Participate in cross-functional team meetings to provide updates on the program and address any issues or concerns * Collaborate cross-functionally with internal stakeholders, including medical affairs, clinical development, regulatory, drug supply, etc. * Adheres to all relevant processes, training, and SOPs to ensure consistency, efficiency, and compliance. * Continued process improvements to ensure consistency, efficiency, and compliance.