Program Management Lead

3 days ago

Menlo Park, California, United States Summit Therapeutics Sub, Inc. Full time
About the Role

We are seeking a highly experienced Program Management Lead to lead our program-level management efforts and impact new indications workstreams, cross-functional activities, and strategic projects.

The successful candidate will bring prior solid tumor oncology pharma knowledge from multiple clinical to commercialization experiences and a strategic mindset to ensure development-business strategy is implemented and works well across global issues.

This role requires an assertive and dynamic management approach, ability to be highly flexible, aptitude for delivering respectful communication in a fast-paced environment, and ability to build teams and take action.

Responsibilities
  • Strategic Program Planning: Implement comprehensive program strategy aligned with organizational goals and to maximize the overall value of ivonescimab, maintaining an overall plan for assigned zones
  • Define program milestones, decision-points, objectives, inflections, and deliverables in collaboration with senior leadership as well as create scenario-based plans and decision-trees
  • Conduct issue/opportunity/risk assessments, participate in strategic planning, and drive decision-quality throughout the program, including building the materials, frameworks, or tools for teams
Qualifications
  • Bachelor's Degree (scientific or healthcare discipline preferred) with at least 7+ years of pharmaceutical / biotech industry experience in a project management role is preferred; MBA desired
  • A minimum of 10+ years of program management experience or Project Management Professional (PMP) certification with equivalent combination of experience is required
  • Prior pharmaceutical drug development experience required
  • Ability to travel to offices with location on the East or West coast time zones; San Francisco Bay area is preferred
  • Comprehensive experience as a pharmaceutical program manager on a product team, past PML experience on numerous molecule sub-teams, and hands-on experience across functions will offer the best opportunity for readiness in this position and is preferred
  • Prior solid tumor oncology disease experience in late-stage drug development and understanding of registrational trials is required; commercialization phase experience a plus
  • Past roles working with R&D, Regulatory, and internal departments is required
  • Experience quickly building strong and sustaining relationships with stakeholders in virtual global channels and in-person; including with senior levels in the organization for drug development, manufacturing, and external partners' activities
  • Collaboration experience working with alliance management and external partners (e.g., co-development, academic centers, international cooperative groups, industry stakeholders) is strongly preferred
  • Demonstrated program management competencies to effectively prioritize, multitask, and execute tasks in a dynamic, fast-paced, collaborative environment where focus and flexibility are essential
  • Ability to integrate all cross-functional perspectives into a successful approach to drive results, managing and/or leading dynamically to meet company goals
  • Demonstrated ability to execute company and product strategy, adaptable to evolving factors, identify process improvements & efficiencies, plus contribute to improving strategy and scenario planning
  • Expertise in MS Office suite (e.g., PowerPoint, Word, Excel, Project), experienced in building presentations for executives and presenting materials, experience using electronic document management systems, document review tools, and expertise in standard project management software (e.g., Smartsheets) required
  • Strong computer skills, organizational skills, and multi-task management
  • Excellent communicator in public-speaking, meeting facilitation, email communication, and in-person

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