Senior CRA II: Medical Device Trials & Site Lead

Fortrea; Iowa; Vor Ort; USD 130.000 - 133.000; Vollzeit

Zusammenfassung

Fortrea's Central-based FSP team is seeking an experienced Senior CRA II for site monitoring and management across clinical studies. The role requires 3+ years of monitoring experience and 1+ year of device-related monitoring, with leadership responsibilities on selected projects.

Travel is a key component, and incumbents will support protocol development, data quality reviews, and regulatory compliance under Fortrea SOPs. Fluency in English and strong communication skills are essential.

Qualifikationen

• University degree in life sciences or related field.
• 3+ years of clinical monitoring experience.
• 1+ year of device experience.
• Fluent in English and local language.
• Knowledge of SAE reporting and data review.

Aufgaben

• Responsible for all aspects of study site monitoring and closeout.
• Liaise with vendors and manage site coordination.
• Prepare trip reports and monitor protocol adherence.
• Lead monitor for a protocol or project as assigned.
• Train and mentor junior staff.

Kenntnisse

Site monitoring

SAE reporting

Regulatory knowledge

Travel readiness

Team leadership

Ausbildung

Life science degree

Jobbeschreibung

Fortrea's Central-based FSP team is seeking an experienced Senior CRA II for site monitoring and management across clinical studies. The role requires 3+ years of monitoring experience and 1+ year of device-related monitoring, with leadership responsibilities on selected projects.

Travel is a key component, and incumbents will support protocol development, data quality reviews, and regulatory compliance under Fortrea SOPs. Fluency in English and strong communication skills are essential.