Senior Oncology CRA - Remote, East Coast Travel

Worldwide Clinical Trials; Milton (MA); A distancia; USD 90.000 - 120.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials, a global CRO, is seeking a Senior Clinical Research Associate to ensure high-quality data and regulatory compliance across East Coast sites. This home-based role supports sites, study teams, and sponsors with leadership, monitoring, and site management throughout the trial lifecycle.

You will travel regionally (approximately 8–10 days per month), qualify investigative sites, support start-up activities, monitor visits, and ensure protocol adherence and patient safety

Formación

• Bachelor's or nursing degree; 5+ years as regional, traveling CRA.
• Experience monitoring Oncology trials; gastric cancer preferred.
• Willingness to travel 8–10 days per month; East Coast-based.

Responsabilidades

• Manage monitoring visits and site management across East Coast.
• Identify and qualify investigative sites for study execution.
• Coordinate start-up activities, regulatory documentation, and budgets.
• Conduct Pre-Site Selection Visits, Study Initiation Visits, Interim Monitoring Visits and Closeout Visits.
• Train site personnel on protocol requirements, data collection, and safety reporting.
• Monitor site performance and provide ongoing support throughout study maintenance.
• Ensure informed consent, safety reporting, and regulatory compliance.

Conocimientos

Travel-ready

Site Monitoring

Regulatory knowledge

Data quality focus

Communication skills

Educación

Bachelor's Degree or Nursing Degree

Descripción del empleo

Worldwide Clinical Trials, a global CRO, is seeking a Senior Clinical Research Associate to ensure high-quality data and regulatory compliance across East Coast sites. This home-based role supports sites, study teams, and sponsors with leadership, monitoring, and site management throughout the trial lifecycle.

You will travel regionally (approximately 8–10 days per month), qualify investigative sites, support start-up activities, monitor visits, and ensure protocol adherence and patient safety