Job Description: We are seeking a growth and improvement minded Value Medical Cross Team Project Manager that can help drive our Strategic Operating Priorities. The goal of the Value Medical Cross Team Project Manager is to provide the Value Medical Project Management (VMPM) Leads specific capability and in-depth knowledge of one or more areas in the execution of the integrated Value Evidence and Medical (VEAM) Plans. The Cross Team Project Manager will be a subject matter expert and key contact for one or more specific elements of the Value Evidence and Medical plan and provide flex capacity to the VEST and SMART teams at various stages of product or program lifecycle, depending on the specific needs of the VEST and SMART teams. This role works closely with the Lead PMs in Value Medical Project Management and the global cross-functional leads in other groups to ensure the seamless coordination and execution of all relevant aspects of the Value Evidence and Medical Plans throughout their product and program lifecycles. The Cross Team PM will work with more than one Lead PM across products and programs. Additional Key Responsibilities • Contribute to aggregation and reporting of internal and external strategic insights (e.g. X-FLY, IRMS, Medical Intelligence Dashboard) to inform the development and execution of Value Evidence and Medical plans • Support the Lead PM with the gathering and synthesis of one or more components of the Value Evidence and Medical plan (e.g., HTA dossiers, Medical Education, input meetings, etc. • Support the planning and coordination of VEAM team meetings, related communications, and community/team site stewardship • Support Lead PMs across therapeutic areas for key congresses in collaboration with other group stakeholders and other internal and external stakeholders • Ad hoc and special project initiatives requiring collaboration and coordination with other project managers across product/programs,, and cross-functional teams (IT, Operations) • Align external stakeholder engagement activities (e.g. EIFs, SIEs, Scientific Leader Utilization Plan (SUP)) across programs and therapeutic areas with key milestones in the Value Evidence and Medical plan. • Track above Value Evidence and Medical project progress and provide project updates/summaries • Team project initiation, budget tracking and vendor activity management • Navigate internal processes and procedures, including compliance and finance, to ensure compliant execution of assigned projects

Responsibilities: We are seeking a growth and improvement minded Value Medical Cross Team Project Manager that can help drive our Strategic Operating Priorities. The goal of the Value Medical Cross Team Project Manager is to provide the Value Medical Project Management (VMPM) Leads specific capability and in-depth knowledge of one or more areas in the execution of the integrated Value Evidence and Medical (VEAM) Plans. The Cross Team Project Manager will be a subject matter expert and key contact for one or more specific elements of the Value Evidence and Medical plan and provide flex capacity to the VEST and SMART teams at various stages of product or program lifecycle, depending on the specific needs of the VEST and SMART teams. This role works closely with the Lead PMs in Value Medical Project Management and the global cross-functional leads in other groups to ensure the seamless coordination and execution of all relevant aspects of the Value Evidence and Medical Plans throughout their product and program lifecycles. The Cross Team PM will work with more than one Lead PM across products and programs. Additional Key Responsibilities • Contribute to aggregation and reporting of internal and external strategic insights (e.g. X-FLY, IRMS, Medical Intelligence Dashboard) to inform the development and execution of Value Evidence and Medical plans • Support the Lead PM with the gathering and synthesis of one or more components of the Value Evidence and Medical p an (e.g., HTA dossiers, Medical Education, input meetings, etc. • Support the planning and coordination of VEAM team meetings, related communications, and community/team site stewardship • Support Lead PMs across therapeutic areas for key congresses in collaboration with other group stakeholders and other internal and external stakeholders • Ad hoc and special project initiatives requiring collaboration and coordination with other project managers across product/programs,, and cross-functional teams (IT, Operations) • Align external stakeholder engagement activities (e.g. EIFs, SIEs, Scientific Leader Utilization Plan (SUP)) across programs and therapeutic areas with key milestones in the Value Evidence and Medical plan. • Track above Value Evidence and Medical project progress and provide project updates/summaries • Team project initiation, budget tracking and vendor activity management • Navigate internal processes and procedures, including compliance and finance, to ensure compliant execution of assigned projects

Qualifications: Education • Bachelor's Degree in life sciences, business, or related healthcare area Experience | Knowledge | Skills Required • 3 (three) years in project management, pharmaceutical, clinical research, outcomes research or medical implementation related field • Work independently and as a Team member with Integrity | Precision | Accomplishment | Motivational Ambition | Respect • Strong interpersonal, verbal, and written communication skills to work with medical and/or scientific teams • Independently handle multiple projects and priorities simultaneously and function in a fast-paced environment • Ability to quickly and comprehensively learn about new subject areas and environments • Self-motivation, flexibility, resourcefulness, and problem-solving capabilities • Outstanding Microsoft Word, PowerPoint, Excel, and Teams skills Preferred • PMP or CAPM certification • Working globally across regions and countries • Leading large complex multi-stakeholder projects • Prior vendor management and budget-planning Additional: Pharma or Biotech industry background. This is not an IT Project Management role. Hybrid role - 3 days onsite required each week. Site location: Rahway, NJ or Upper Gwynedd PA.