Senior Oncology CRA – Midwest (Remote/Home-Based)

Worldwide Clinical Trials; Illinois; Remote; USD 90,000 - 125,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate (CRA) to support Midwest-based sites in a home-based role. The position involves traveling ~8–10 days per month to investigate sites, ensuring protocol adherence, quality data, and patient safety across studies.

The Senior CRA partners with sites, study teams, and sponsors to lead monitoring visits, start-up activities, and regulatory compliance, with emphasis on oncology trials and full-service monitoring.

Qualifications

• Bachelor's Degree or a Nursing Degree, plus 5+ years as a regional, traveling Clinical Research Associate.
• 2 years of required experience monitoring Oncology clinical trials.
• Requires travel within the specified region; 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

Site monitoring

Regulatory knowledge

Clinical trial coordination

Education

Bachelor's or Nursing degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate (CRA) to support Midwest-based sites in a home-based role. The position involves traveling ~8–10 days per month to investigate sites, ensuring protocol adherence, quality data, and patient safety across studies.

The Senior CRA partners with sites, study teams, and sponsors to lead monitoring visits, start-up activities, and regulatory compliance, with emphasis on oncology trials and full-service monitoring.