Senior CRA - Oncology Trials | Remote/Home-Based, Midwest

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

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee clinical study activities across Midwest sites. The role focuses on quality, patient safety and regulatory compliance, acting as a partner to sites, study teams, and sponsors to drive data accuracy and study success.

The position requires 5+ years as a regional traveling CRA with Oncology trial monitoring experience, and the ability to travel regionally 8-10 days per month.

Qualifications

• 5+ years as a regional traveling CRA.
• Experience monitoring Oncology trials.
• Willingness to travel 8-10 days per month.
• Experience in full-service monitoring preferred.

Responsibilities

• Manage clinical research activities at investigative sites participating in Worldwide clinical studies.
• Identify and assess potential research sites to support successful study execution.
• Coordinate study start-up activities, including collection of regulatory documentation and support of contract and budget processes.
• Conduct all types of monitoring visits: PSSVs, SIVs, IMVs and COVs.
• Train site personnel on protocol requirements, data collection processes, and safety reporting expectations.
• Monitor site performance and provide ongoing support throughout study maintenance activities.
• Ensure compliance with informed consent requirements, safety reporting obligations, and applicable regulatory standards.
• Partner with sites and study teams to drive data quality, participant safety, and overall study success.
• Support site closeout activities and ensure study requirements are completed at the conclusion of the trial.

Skills

Clinical trial monitoring

Regulatory compliance

Site management

Travel readiness

Education

Bachelor's degree or Nursing degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee clinical study activities across Midwest sites. The role focuses on quality, patient safety and regulatory compliance, acting as a partner to sites, study teams, and sponsors to drive data accuracy and study success.

The position requires 5+ years as a regional traveling CRA with Oncology trial monitoring experience, and the ability to travel regionally 8-10 days per month.