Senior CRA II: Medical Device Trials Lead

Fortrea

Missouri

Vor Ort

USD 130.000 - 133.000

Vollzeit

Vor 7 Tagen
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Zusammenfassung

Fortrea seeks an experienced Senior CRA II based in the Central/Midwest region (Missouri) to lead site monitoring and site management for clinical studies. You will ensure protocol adherence, data integrity, and regulatory compliance while coordinating with project teams and vendors.

Requirements include a life science degree and at least 3 years of monitoring experience, plus 1+ year of device experience. Expect significant travel (60-80%), with opportunities to mentor junior staff and

Qualifikationen

  • Bachelor's degree or life science certification preferred.
  • 3+ years of clinical monitoring experience.
  • 1+ year of device experience is required.

Aufgaben

  • Monitor and manage clinical sites, ensure protocol compliance and data integrity.
  • Lead monitoring plans and trip reports; coordinate with Project Manager/Director.
  • Oversee site readiness, regulatory adherence, and SAE reporting.

Kenntnisse

Site monitoring
Clinical monitoring
SAE reporting
Team leadership

Ausbildung

Life science degree

Jobbeschreibung

Fortrea seeks an experienced Senior CRA II based in the Central/Midwest region (Missouri) to lead site monitoring and site management for clinical studies. You will ensure protocol adherence, data integrity, and regulatory compliance while coordinating with project teams and vendors.

Requirements include a life science degree and at least 3 years of monitoring experience, plus 1+ year of device experience. Expect significant travel (60-80%), with opportunities to mentor junior staff and

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