Senior Oncology CRA - Remote, Regional Travel Lead

Worldwide Clinical Trials Holdings, Inc.; North Carolina; Hybrid; USD 97,000 - 193,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate (CRA) to oversee site activities, ensure regulatory compliance, and drive data quality across oncology studies. This home-based role supports sites in the Southeast and Mid-Atlantic, with regular regional travel to investigator sites.

You will partner with study teams, monitor performance, and train site personnel on protocol requirements, data collection, safety reporting, and regulatory standards throughout the trial

Qualifications

• Bachelor's Degree or Nursing Degree required.
• 5+ years as regional, traveling Clinical Research Associate.
• Experience monitoring Oncology trials.
• Willingness to travel regionally (Southeast / Mid-Atlantic).

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 regulatory documentation and support of contract and budget processes.
• Conduct all types of monitoring visits: PSSVs, SIVs, IMVs, COVs.
• Train site personnel on protocol requirements, data collection, and safety reporting expectations.
• Monitor site performance and provide ongoing support throughout study maintenance activities.
• Ensure compliance with informed consent, safety reporting, and regulatory standards.
• Partner with sites and study teams to drive data quality and participant safety.

Skills

Oncology trials experience

Site monitoring

Travel within region

Full-service monitoring

Team collaboration

Education

Bachelor's Degree or Nursing Degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate (CRA) to oversee site activities, ensure regulatory compliance, and drive data quality across oncology studies. This home-based role supports sites in the Southeast and Mid-Atlantic, with regular regional travel to investigator sites.

You will partner with study teams, monitor performance, and train site personnel on protocol requirements, data collection, safety reporting, and regulatory standards throughout the trial