Strategic Director, Clinical Quality & Research Programs

Novant Health

Charlotte (NC)

Vor Ort

USD 150.000 - 190.000

Vollzeit

14 Tage+

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Zusammenfassung

Novant Health seeks a Director of Clinical Quality and Research Programs to lead the Abdominal Wall Reconstruction & Hernia Center's research and quality initiatives. The role will engage patients, guide consent, support recruitment, and coordinate follow-up while shaping the research infrastructure and clinical outcomes.

Responsibilities include strategic program development, operational oversight, and external partnerships, with emphasis on GCP/ICH/FDA/IRB compliance and responsible

Qualifikationen

  • 5 years of clinical trials experience required.
  • 5 years of management experience required.
  • ACRP or SoCRA certification (or must be obtained within 18 months of hire) required.
  • Operational knowledge of GCP, ICH, FDA, and IRB standards across sponsored and investigator-initiated research.

Aufgaben

  • Provide strategic leadership and direction for the specialty research program and infrastructure.
  • Direct operational performance of the research program including workflows, recruitment strategies, data systems, and study implementation.
  • Build and maintain partnerships with physicians, nursing leaders, research teams, and IRB.
  • Ensure compliance with regulatory standards and sponsor requirements across projects.
  • Oversee program resources, staffing models, and budgets for growth and expansion.

Kenntnisse

Strategic leadership
Program development
Clinical trial management
Data analytics
IRB compliance

Ausbildung

Bachelor's Degree
Graduate Degree (Health Science)

Jobbeschreibung

Novant Health seeks a Director of Clinical Quality and Research Programs to lead the Abdominal Wall Reconstruction & Hernia Center's research and quality initiatives. The role will engage patients, guide consent, support recruitment, and coordinate follow-up while shaping the research infrastructure and clinical outcomes.

Responsibilities include strategic program development, operational oversight, and external partnerships, with emphasis on GCP/ICH/FDA/IRB compliance and responsible

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