M

Medpace

Global CRO delivering full-service clinical trials

Senior Director - IT Project Management Office

IT Project ManagementConfirmed live in the last 24 hours
Full-timeCincinnati, OH, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in Information Technology, Computer Science, Business Administration, or a related field is required; a master's degree is preferred.
  • At least 10 years of experience in IT project management, including at least 3 years in a leadership role managing project managers, business analysts, or a PMO.
  • Experience establishing or maturing PMO processes, governance frameworks, and project standards.
  • Strong knowledge of software development lifecycle methodologies, including Agile, Waterfall, and hybrid approaches.
  • Experience managing a portfolio of concurrent software projects, including budgets, resource planning, and risk management.
  • Ability to communicate effectively with executives, business stakeholders, and technical teams.
  • Strong leadership, coaching, and conflict resolution skills.
  • Proficiency with project and portfolio management tools and reporting platforms.

Responsibilities

  • Lead, mentor, and develop a team of IT project managers and business analysts, including hiring, performance management, and career development.
  • Allocate project manager and business analyst resources across projects based on priorities, complexity, and team capacity.
  • Foster accountability, continuous improvement, and collaboration between project management and engineering teams.
  • Establish, document, and maintain project management methodologies, standards, templates, and best practices across Agile, Waterfall, and hybrid approaches.
  • Define and enforce project governance, including stage gates, approval processes, change control, and escalation paths.
  • Ensure software development projects meet regulatory, quality, and data integrity requirements applicable to a contract research organization environment, including GxP, 21 CFR Part 11, and validation requirements.
  • Partner with Validation and Quality Assurance teams to align PMO processes with software development lifecycle, computer system validation, and audit-readiness expectations.
  • Conduct periodic project health checks and audits to confirm adherence to PMO standards.
  • Own the IT project portfolio, including intake, prioritization, and roadmap planning in collaboration with IT and business leadership.
  • Develop and deliver portfolio dashboards, status reports, and key performance metrics to senior leadership.
  • Oversee portfolio-level resource forecasting and capacity planning.
  • Identify cross-project dependencies, risks, and conflicts, and drive resolution at the portfolio level.
  • Define PMO strategy, goals, and maturity roadmap aligned with IT and corporate objectives.
  • Select, implement, and administer project and portfolio management tools, such as Jira, Azure DevOps, Smartsheet, and Microsoft Project.
  • Lead post-project reviews and use lessons learned to refine processes and improve delivery outcomes.
  • Serve as an escalation point for high-risk or high-visibility projects and provide direct project oversight when needed.

Desired Qualifications

  • PMP, PgMP, PfMP, SAFe, or another relevant certification.
  • Experience in a contract research organization, pharmaceutical, biotech, or other regulated life sciences environment.
  • Working knowledge of GxP, 21 CFR Part 11, HIPAA, and computer system validation practices.
  • Experience overseeing custom, internally developed software projects rather than only vendor or commercial off-the-shelf implementations.
  • Experience with organizational change management and driving adoption of new processes across teams.
  • Familiarity with portfolio management tools and data visualization or reporting tools, such as Power BI and Tableau.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

Recently Posted Jobs

Explore more opportunities at Medpace

See more jobs