Senior Oncology CRA - Remote (West Coast, Travel)

Worldwide Clinical Trials; Arizona; A distancia; USD 97.000 - 193.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee site activities across the West Coast, ensuring high-quality, compliant trial conduct and data integrity. This home-based role partners with investigative sites, study teams, and sponsors to deliver reliable results.

You will monitor sites, qualify investigators, manage start-up, and conduct visits (PSSV, SIV, IMV, COV). A Bachelor's or Nursing degree with 5+ years as a regional CRA and oncology trial experience

Formación

• Bachelor's or Nursing degree required with 5+ years as a regional traveling Clinical Research Associate.
• Experience monitoring Oncology/Hematology trials.
• Must travel within the specified region; 8–10 days per month.
• Experience in full-service monitoring is preferred.
• Strong knowledge of clinical trial processes, site management, and regulatory requirements.

Responsabilidades

• Manage clinical research activities at investigative sites in Worldwide studies.
• Identify and assess potential research sites to support study execution.
• Coordinate start-up activities and support regulatory documentation & contracts.
• Conduct monitoring visits (PSSV, SIV, IMV, COV).
• Train site personnel on protocol requirements, data collection, and safety reporting.
• Monitor site performance and provide ongoing study support.
• Ensure informed consent and safety reporting compliance.
• Support site closeout activities and study completion.

Conocimientos

Clinical monitoring

Site management

Regulatory compliance

Travel readiness

Oncology experience

Educación

Bachelor's or Nursing degree

Descripción del empleo

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee site activities across the West Coast, ensuring high-quality, compliant trial conduct and data integrity. This home-based role partners with investigative sites, study teams, and sponsors to deliver reliable results.

You will monitor sites, qualify investigators, manage start-up, and conduct visits (PSSV, SIV, IMV, COV). A Bachelor's or Nursing degree with 5+ years as a regional CRA and oncology trial experience