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Senior Director, Data Delivery and Insights

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Senior Director, Data Delivery and Insights

India - Hyderabad APLICAR AHORA
ID de la oferta R-235500 País: India - Hyderabad Estado: On Site Fecha de publicación Feb. 25, 2026 CATEGORÍA DE EMPLEO: Clinical Development

ABOUT AMGEN

Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today.

ABOUT THE ROLE

Role Description:

The Senior Director Data Delivery & Insights sets and drives the enterprise-level data delivery strategy across one or more therapeutic areas, ensuring scalable, future-ready data operating models that enable accelerated development decisions, regulatory submissions, and portfolio value realization. This role shapes the long-term data management vision, operating model, and capability roadmap, aligning therapeutic area priorities with enterprise transformation goals.

The Senior Director leads and develops large therapeutic area teams by managing Program Data Delivery Leads, fostering consistency in ways of working, acting as the point of escalation, and building a culture of accountability, collaboration, and continuous improvement across the therapeutic area.

This critical leader represents the therapeutic area as the senior data management voice, partnering cross-functionally with GDO and non-GDO stakeholders to reflect enterprise strategy, contribute therapeutic area perspectives to global initiatives, and ensures Amgen’s data management strategy is consistently applied.

Roles & Responsibilities:

  • Accountable for data delivery performance across multiple therapeutic areas or a high complexity/global portfolio, ensuring alignment to enterprise strategy and consistent execution standards across the organization.
  • Sets the therapeutic area data delivery strategy and ways of working and align study teams to it.
  • Review and approves program-level data management plans, integrated data review approaches, and lock plans across the TA.
  • Run TA delivery forums to compare studies, surface risks, and drive consistent practices across Program Data Delivery Leads, Study Data Delivery Leads, and Central Monitors.
  • Prioritize and allocate Study Data Delivery Leads, Central Monitors, and support resources across the TA based on risk and milestones.
  • Track TA-level delivery metrics (database readiness, LPLV-to-lock cycle time, unlocks, query aging) and drive corrective actions.
  • Escalate cross-study issues and remove roadblocks with Clinical Operations, Biostats, Safety, and Systems teams.
  • Lead and develop a layered leadership structure (Directors, Program Data Delivery Leads), building succession pipelines and long-term capability strategy for the function
  • Harmonize KRI/QTL usage and IDRP conventions across the TA in partnership with stakeholders.
  • Collaborate with peers to evolve the global data delivery operating model
  • Lead TA readiness for interim and final analyses, chairing lock readiness reviews and aligning dependencies.
  • Represent the TA in governance and portfolio reviews, communicating status, risks, and decisions.
  • Develop annual group goals and manage resource and budget for the TA.

Basic Qualifications and Experience:

  • Doctorate Degree and 20+ years of life science, computer sciences, business administration experience OR
  • Master’s Degree or Bachelor’s degree and 22 years of life science, computer sciences, business administration experience

In addition to meeting at least one of the above requirements, you must have a minimum of 10 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources.  Your managerial experience may run concurrently with the required technical experience referenced above.

Preferred Experience:

  • 12+ years work experience in life sciences industry, particularly focusing on clinical trial work, including 10+ years of biopharmaceutical clinical research experience obtained at a biotech or pharmaceutical company
  • Experience managing multiple teams / direct reports across multiple geographies
  • Experience at or oversight of outside clinical research vendors (CRO’s, central labs, imaging vendors, etc.)

Functional Competencies:

Must-Have Competencies:

  • Experience leading cross-functional / cross-geography / cross-trial teams, ensuring operational excellence and smooth decision-making; ability to escalate and resolve challenges in alignment with global study strategy priorities.
  • Proficient in overseeing resource and budget allocation in adherence to functional financial principles for optimal, cost effective resource planning in aligned to global clinical priorities.
  • Experience in delivering large complex portfolio/cross-study level, budgets, timelines, and performance metrics (time, cost, quality) aligned to global / functional priorities.
  • Demonstrates clear understanding of how to build collaborative networks across cross-functional teams, senior management, and external stakeholders, internally and externally to drive efficiency across processes.
  • Experience in assessing internal capabilities and identifying key capabilities to build training content, monitoring skill improvement, and drive competency builds across function and within teams.
  • Experience driving and leading organizations through​ cross-functional change initiatives such as identifying solutions to problems and innovating and change strategies and structure to meet future needs.
  • Big picture, pro-active thinking with the ability to assess broad impacts across complex multiple product portfolios to identify innovative solutions.
  • Ability to consolidate and interpret global data trends and apply those in strategic design and decision-making for a complex clinical portfolio.
  • Proficient in driving and leading continuous improvement initiatives for team's working practices, ensuring cross-functional adoption of new processes.
  • Experience in establishing strategic partnerships with external vendors at an enterprise / portfolio level ensuring optimized utilization of external resources.

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