Oncology Senior CRA – Midwest | Remote Home-Based

Worldwide Clinical Trials; Indiana; Remote; USD 90,000 - 130,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee site monitoring and trial execution across the Midwest. You will work remotely with travel to investigative sites, ensuring data quality, patient safety, and regulatory compliance throughout the study lifecycle.

The role emphasizes regional travel (approx. 8-10 days per month), start-up coordination, visits PSSV/SIV/IMV/COV, and collaboration with study teams and sponsors.

Qualifications

• Bachelor's Degree or Nursing Degree with 5+ years as a regional, traveling CRA.
• Minimum 2 years monitoring Oncology trials.
• Willingness to travel within the Midwest regional area; full-service monitoring experience preferred.
• Strong knowledge of clinical trial processes and regulatory requirements.

Responsibilities

• Manage clinical research activities at investigative sites across Worldwide trials.
• Identify and assess research sites to support study execution.
• Coordinate start-up activities and regulatory documentation.
• Conduct monitoring visits (PSSV, SIV, IMV, COV) and train site staff.
• Ensure protocol adherence, data quality, and patient safety throughout the trial.

Skills

Clinical trial monitoring

Site management

Regulatory compliance

Travel readiness

Education

Bachelor's or Nursing degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee site monitoring and trial execution across the Midwest. You will work remotely with travel to investigative sites, ensuring data quality, patient safety, and regulatory compliance throughout the study lifecycle.

The role emphasizes regional travel (approx. 8-10 days per month), start-up coordination, visits PSSV/SIV/IMV/COV, and collaboration with study teams and sponsors.