Senior Oncology CRA — West Coast Remote Role

Worldwide Clinical Trials; Washington; Remote; USD 97.000 - 193.000; Vollzeit

Zusammenfassung

Worldwide Clinical Trials is a home-based role on the West Coast of the United States for a Senior CRA. The role supports sites across the region with travel about 8–10 days per month, collaborating with sponsors and global teams to ensure protocol adherence and high-quality data.

You will lead site management, review regulatory documentation, and drive data quality and patient safety throughout the trial lifecycle.

Qualifikationen

• Bachelor's Degree or a Nursing Degree.
• 5+ years as a regional, traveling Clinical Research Associate.
• Experience monitoring Oncology (Hematology experience preferred).
• Requires travel within the specified region; 8–10 DOS monthly.
• Experience in full-service monitoring and site management with regulatory knowledge.

Aufgaben

• Manage clinical research activities at investigative sites participating in Worldwide studies.
• Identify and assess potential research sites to support study execution.
• Coordinate study start-up activities including regulatory documentation support.
• Conduct all monitoring visits (PSSVs, SIVs, IMVs, COVs).
• Train site personnel on protocol, data collection, and safety reporting expectations.
• Monitor site performance and provide ongoing support during maintenance.
• Ensure informed consent, safety reporting, and regulatory compliance.
• Support site closeout activities to complete trial requirements.

Kenntnisse

Site management

Clinical monitoring

Regulatory knowledge

Travel readiness

Ausbildung

Bachelor's Degree

Nursing Degree

Jobbeschreibung

Worldwide Clinical Trials is a home-based role on the West Coast of the United States for a Senior CRA. The role supports sites across the region with travel about 8–10 days per month, collaborating with sponsors and global teams to ensure protocol adherence and high-quality data.

You will lead site management, review regulatory documentation, and drive data quality and patient safety throughout the trial lifecycle.