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Global drug and device development services

Senior Director, Clinical Project Management - Clinical Project Management Centre of Excellence

Program ManagementUpdated on Nov 12
Full-time

About the Job

Requirements

  • Extensive global clinical trial delivery experience across the full study lifecycle, including start-up, conduct, and closeout, with personal accountability for scope, timelines, financials, risk, resources, vendors, sponsors, and quality.
  • Significant senior leadership experience within project management, a Project Management Office, or a comparable enterprise capability function in a global, matrixed clinical development or contract research organization environment.
  • Experience designing and owning a role-based competency framework and structured onboarding and continuous-learning pathway for clinical project-leadership roles, with demonstrated adoption and measurable impact.
  • Experience establishing enterprise project-management standards across functions outside direct line authority, including the governance, decision rights, and accountability mechanisms needed to drive sustained adoption.
  • Experience building and leading a distributed capability network, such as certified champions, subject-matter experts, or train-the-trainer communities, that enables central standards to be delivered consistently within individual functions.
  • Working knowledge of International Council for Harmonisation Good Clinical Practice, clinical trial regulatory and quality requirements, inspection readiness, and corrective and preventive action; ability to influence at executive level and lead effectively through a complex matrix.
  • Experience establishing a Project Management Centre of Excellence or leading a significant operating-model transformation, with demonstrated improvements in study start-up, site activation, closeout, quality, or cycle-time performance.
  • Experience using learning platforms, analytics, digital or artificial-intelligence-enabled solutions to scale capability and measure effectiveness.
  • Experience using process-engineering principles to design and embed standardized, scalable project-management processes across a complex global organization, supported by clear controls, performance measures, and continuous improvement.
  • Must live in the Eastern or Midwest United States, Canada, or Ireland and be able to travel 10%.
  • Bachelor’s degree in life sciences, business, project management, or a related discipline, or an equivalent combination of education and relevant professional experience.

Responsibilities

  • Lead the strategy, operating model, charter, and roadmap for the federated Project Management Centre of Excellence, defining central ownership, local delivery responsibilities, and decision rights.
  • Establish and govern enterprise project-management standards, methodologies, processes, templates, systems, and certification requirements for clinical trial delivery.
  • Design and own a role-based competency framework, structured onboarding journey, and continuous-learning architecture covering project-leadership roles across the organization.
  • Build, train, and certify a distributed network of functional champions and subject-matter experts, securing the protected capacity and governance needed to deliver central standards consistently at a local level.
  • Standardize study intake and outtake processes and drive measurable improvements in study start-up, site activation, closeout, quality, and cycle-time performance.
  • Establish governance, adoption measures, scorecards, and accountability mechanisms that embed standards across functions, divisions, and geographies.
  • Partner with Quality and Oversight, Governance and Oversight, Data Analytics, Business Transformation, and Digital and AI teams to scale capability, strengthen process effectiveness, and demonstrate measurable business value.
  • Engage senior executives and delivery leaders, positioning project-management capability as a driver of quality, operational performance, sponsor experience, and business growth.
  • Build, lead, and develop a high-performing central team, with accountability for resource planning, priorities, and stakeholder management.

Desired Qualifications

  • Relevant credentials such as Project Management Professional, Program Management Professional, Prosci, or continuous-improvement qualifications are an advantage.

About the Company

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Global drug and device development services

This company provides consulting, development, and commercialization support for drugs and medical devices through a global network of offices. Its team across 53 countries offers end-to-end services, from strategy and regulatory work to manufacturing and market access, helping clients shorten development time, lower costs, and raise quality. It differentiates itself with wide geographic reach and a clear focus on reducing time to market and cost while leveraging deep experience across many therapeutic areas. Its goal is to help clients accelerate the development of life-saving products and improve quality of life by delivering reliable information, practical solutions, and solid performance.

Company size
10,001+
Company stage
IPO
Headquarters
Ireland
Founded
1990

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