Senior Oncology CRA – Remote (Western US Travel)

Worldwide Clinical Trials; Arizona; Remote; USD 97,000 - 193,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee site monitoring and regulatory compliance for oncology studies. This home-based role supports Western US sites, coordinating visits and ensuring data quality and protocol adherence.

You will work with study teams and sponsors, leading monitoring activities and mentoring site personnel while traveling 8–10 days per month. The role emphasizes quality, safety, and timely study delivery.

Qualifications

• Bachelor's or Nursing degree with 5+ years as a regional traveling CRA.
• Required experience monitoring Oncology clinical trials.
• Willingness to travel 8–10 days per month; some remote visits.
• Experience in full-service monitoring is preferred.
• Strong knowledge of clinical trial processes, site management, and regulatory requirements.

Responsibilities

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

Skills

Clinical research experience

Traveling/Regional CRA

Oncology monitoring

Regulatory knowledge

Education

Bachelor's degree or Nursing degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee site monitoring and regulatory compliance for oncology studies. This home-based role supports Western US sites, coordinating visits and ensuring data quality and protocol adherence.

You will work with study teams and sponsors, leading monitoring activities and mentoring site personnel while traveling 8–10 days per month. The role emphasizes quality, safety, and timely study delivery.