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Medpace

Global CRO delivering full-service clinical trials

Internal Audit Manager

Internal Audit & ControlsConfirmed live in the last 24 hours
Full-timeCincinnati, OH, USANo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in Accounting, Finance, Business, or a related field.
  • Five to eight years of relevant internal audit, external audit, Sarbanes-Oxley (SOX), risk, or controls experience.
  • Prior supervisory experience and demonstrated experience leading complex audit engagements.
  • Strong knowledge of SOX, internal controls, risk assessment, and professional auditing standards.
  • Strong analytical, judgment, communication, and interpersonal skills.

Responsibilities

  • Plan, manage, and supervise financial, operational, SOX, and other risk-based audit and advisory engagements.
  • Assess complex processes and systems to identify risks and controls, and develop audit procedures and testing plans.
  • Review audit workpapers, findings, conclusions, and reports to ensure audit work is accurate, appropriately supported, and completed in accordance with Internal Audit methodologies.
  • Communicate audit results and practical recommendations to management, and monitor remediation of identified issues.
  • Manage assigned Internal Audit projects and coordinate activities with process owners, external auditors, and other stakeholders.
  • Supervise, mentor, and develop Internal Audit team members, including delegation of work, performance evaluations, training, and participation in hiring.
  • Support risk assessment, audit planning, Internal Audit methodology, and continuous improvement activities.

Desired Qualifications

  • CPA, CIA, CISA, or CISSP certification, or an MBA.
  • Public accounting or external audit experience.

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

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