Senior Oncology CRA – Midwest (Remote + Travel)

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

Job summary

Worldwide Clinical Trials is seeking a Senior CRA to lead high-quality data collection and regulatory compliance across Midwest sites. You will monitor studies from site qualification through closeout, building strong partner relationships with investigators, teams, and sponsors.

Travel will be regional, with 8–10 days per month typical, and oncology monitoring expertise is required. The role emphasizes leadership, data quality, and adherence to protocol in a supportive, inclusive environment

Qualifications

• Bachelor's Degree or Nursing Degree required.
• 5+ years as a regional, traveling Clinical Research Associate.
• 2 years of experience monitoring Oncology clinical trials.

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 research monitoring

Site management

Regulatory compliance

Travel flexibility

Education

Bachelor's Degree or Nursing Degree

Job description

Worldwide Clinical Trials is seeking a Senior CRA to lead high-quality data collection and regulatory compliance across Midwest sites. You will monitor studies from site qualification through closeout, building strong partner relationships with investigators, teams, and sponsors.

Travel will be regional, with 8–10 days per month typical, and oncology monitoring expertise is required. The role emphasizes leadership, data quality, and adherence to protocol in a supportive, inclusive environment