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University of Pennsylvania

Ivy League university in Philadelphia, PA

Associate Director - Radiology IND/IDE Support Office

Clinical Research Operations +1Confirmed live in the last 24 hours
Full-timePhiladelphia, PA, USA$80.9k - $110k /yr

About the Job

Requirements

  • A bachelor's degree in a scientific or related discipline (B.S. or B.A.) and 7–10 years of experience as a monitor, or an equivalent combination of education and experience, are required.
  • Experience supporting FDA-regulated clinical research, including Investigational New Drug and/or Investigational Device Exemption studies, is required.
  • Demonstrated knowledge of FDA regulations, monitoring, guidance, and compliance requirements applicable to clinical research is required.

Responsibilities

  • Oversee FDA regulatory, safety, and compliance activities for Investigational New Drug and Investigational Device Exemption studies.
  • Lead monitoring oversight to ensure compliance, data integrity, and participant safety under FDA and institutional guidelines.
  • Supervise regulatory staff, a team of fewer than 10 individuals.
  • Lead cross-functional teams and serve as a subject matter expert in compliance and monitoring for the IND/IDE Radiology portfolio.
  • Direct the daily operations of the IND/IDE Support Office and serve as the primary FDA liaison.
  • Oversee regulatory submissions, including IND/IDE applications, amendments, annual reports, safety reports, and associated FDA forms.
  • Develop and implement risk-based monitoring plans; oversee monitoring visits and audits; review source documentation and study data; identify compliance risks; and ensure timely corrective and preventive actions.
  • Ensure protocol compliance, subject safety, data integrity, and inspection readiness across active and pending IND/IDE studies.
  • Lead the preparation, review, and submission of FDA regulatory documents, including Forms FDA 1571 and 1572, IND and IDE applications, protocol amendments, annual reports, safety reports, and other required regulatory filings.
  • Lead quality assurance and compliance initiatives, prepare research teams for FDA inspections and audits, and ensure adherence to FDA regulations, Good Clinical Practice, institutional policies, and standard operating procedures.
  • Collaborate with investigators, faculty, and institutional leadership to support efficient, compliant, and high-quality clinical research operations.

Desired Qualifications

  • A master's degree and 5–6 years of relevant experience are preferred.

About the Company

University of Pennsylvania

Ivy League university in Philadelphia, PA

The University of Pennsylvania is a private Ivy League research university in Philadelphia. It comprises twelve undergraduate, graduate, and professional schools, including the Wharton School, Perelman School of Medicine, and Penn Carey Law.

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