Senior Oncology CRA - Midwest (Remote)

Worldwide Clinical Trials; Indianapolis (IN); Remote; USD 97,000 - 193,000; Full time

Job summary

Worldwide Clinical Trials seeks a Senior Clinical Research Associate (CRA) to lead monitoring and site management across studies. You will ensure protocol adherence, patient safety, and regulatory compliance while partnering with sponsors and investigative sites to deliver high-quality data.

The role is home-based, supporting sites across the Midwest with regular regional travel to sites (approximately 8–10 days per month).

Qualifications

• Bachelor's degree or Nursing degree required.
• 5+ years as a regional, traveling CRA.
• 2 years monitoring Oncology trials required.
• Travel within the Midwest US; 8–10 days of site visits monthly.

Responsibilities

• Manage clinical research activities at investigative sites in Worldwide studies.
• Identify and assess potential research sites to ensure study readiness.
• Coordinate start-up activities and regulatory documentation.
• Conduct monitoring visits: PSSVs, SIVs, IMVs, COVs.
• Train site staff on protocol, data collection, and safety reporting.
• Monitor site performance and provide ongoing study support.
• Ensure informed consent, safety reporting, and regulatory compliance.
• Collaborate with sites and study teams to drive data quality.
• Support site closeout and final trial completion.

Skills

Traveling CRA

Oncology trials

Site management

Regulatory knowledge

Education

Bachelor's or Nursing degree

Job description

Worldwide Clinical Trials seeks a Senior Clinical Research Associate (CRA) to lead monitoring and site management across studies. You will ensure protocol adherence, patient safety, and regulatory compliance while partnering with sponsors and investigative sites to deliver high-quality data.

The role is home-based, supporting sites across the Midwest with regular regional travel to sites (approximately 8–10 days per month).