Home-Based Oncology CRA II — Clinical Trials Monitor

Worldwide Clinical Trials Limited spółka z ograniczoną odpowiedzialnością; North Carolina; Hybrid; USD 80.000 - 159.000; Vollzeit

Zusammenfassung

Worldwide Clinical Trials is seeking a Clinical Research Associate II to ensure high‑quality, compliant clinical studies. You will oversee site qualification, initiation, monitoring, and close‑out activities, partnering with investigators as we advance important research programs.

This home‑based position supports US sites; travel is expected 8–10 days per month, with regional focus. You will train site personnel, manage data quality, and ensure regulatory compliance throughout the study

Qualifikationen

• Requires monitoring clinical trials experience.
• Strong knowledge of clinical trial processes and site management.
• Willingness to travel regionally to US sites 8–10 days per month.

Aufgaben

• Conduct site qualification, initiation, monitoring, and close‑out visits per protocol and GCP.
• Evaluate site feasibility and readiness for trial execution.
• Maintain essential regulatory and study documentation for inspection readiness.
• Train and support site personnel on protocol requirements and data quality.
• Verify source data and ensure safety and data integrity.
• Collaborate with sites to resolve data queries and support timely deliverables.
• Monitor investigational product accountability and site files.
• Prepare visit reports for Trial Master File updates.
• Contribute to protocol/CRF/monitoring plan development as needed.

Kenntnisse

Site management

Regulatory knowledge

GCP/compliance

Ausbildung

Bachelor’s Degree or Nursing Degree

Jobbeschreibung

Worldwide Clinical Trials is seeking a Clinical Research Associate II to ensure high‑quality, compliant clinical studies. You will oversee site qualification, initiation, monitoring, and close‑out activities, partnering with investigators as we advance important research programs.

This home‑based position supports US sites; travel is expected 8–10 days per month, with regional focus. You will train site personnel, manage data quality, and ensure regulatory compliance throughout the study