Director Global Integrated Evidence Planning at Dexcom

, , United States -

Full Time

Start Date

Immediate

Expiry Date

12 Jan, 26

Salary

0.0

Posted On

14 Oct, 25

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Project Management, Strategic Planning, Evidence Generation, Research Design, Stakeholder Engagement, Communication, Risk Management, Cross-Functional Collaboration, Medical Knowledge, Publication Planning, Decision Making, Adaptability, Accountability, Team Leadership, Commercial Objectives, Scientific Objectives

Industry

Medical Equipment Manufacturing

Description

Meet the team: Global Integrated Evidence Planning (IEP) is a high-impact function at Dexcom, shaping the future of evidence strategy across the product lifecycle. The IEP team works cross-functionally to anticipate stakeholder needs, evaluate the competitive landscape, and deliver integrated evidence plans that support Dexcom's mission to improve lives through innovative diabetes care. As a Director in the Global IEP team, you will play a pivotal leadership role, translating complex business priorities into actionable evidence strategies that guide enterprise decision-making. You will collaborate across clinical, commercial, and access teams to ensure evidence plans are comprehensive, relevant, and aligned with global objectives. This is a unique opportunity to lead strategically, influence outcomes, and contribute meaningfully to Dexcom's growth and impact. Where you come in: You will lead the development of strategic evidence plans that define business problems, articulate clear objectives, and propose fit-for-purpose evidence generation approaches. You will translate complex information into actionable strategies, anticipate risks, and develop mitigation plans to ensure successful execution. You will establish and operationalize planning frameworks that guide evidence strategy development, ensuring consistency and alignment with business priorities and cross-functional dependencies. You will define and maintain a structured cadence for progress reviews, stakeholder engagement, and decision checkpoints to ensure accountability and momentum. You will apply deep scientific and medical knowledge to critically evaluate existing and emerging evidence, adapting plans to reflect new information. You will contribute to publication and medical communication planning and ensure ongoing assessment of evidence effectiveness and alignment with strategic goals. You will Facilitate strategic discussions to identify priority business objectives and incorporate stakeholder input into planning and execution. What makes you successful: You independently manage complex projects with structured planning, resource coordination, and consistent progress updates to stakeholders. You anticipate challenges and proactively adjust strategies, escalating issues early to maintain momentum and ensure delivery of high-quality outcomes. You operate seamlessly across interdependent work models, including clinical, commercial, and access teams. You ensure deliverables are strategically aligned, outcome-driven, and support enterprise decision-making. You communicate with impact, ensuring content is synthesized, relevant, and tailored to the audience and business context. You build and maintain effective relationships with key stakeholders and collaborate with cross-functional leaders to secure inputs and alignment. You bring experience in evidence generation, and research design. You have knowledge of RWE and its application to commercial and scientific objectives. What you'll get: A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community. A full and comprehensive benefits program. Growth opportunities on a global scale. Access to career development through in-house learning programs and/or qualified tuition reimbursement. An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve. Travel Required: 0-5% Experience and Education Requirements: Typically requires a Bachelor's degree with 15+ years of industry experience 9+ years of successful management experience in relevant industry Remote Workplace: Your location will be a home office; you are not required to live within commuting distance of your assigned Dexcom site (typically 75 miles/120km). If you reside within commuting distance of a Dexcom site (typically 75 miles/120km) a hybrid working environment may be available. Ask about our Flex workplace option.

Responsibilities

Lead the development of strategic evidence plans that define business problems and propose evidence generation approaches. Collaborate across teams to ensure evidence plans are comprehensive and aligned with global objectives.