Senior CRA – Oncology Trials (Remote, East Coast Travel)

Worldwide Clinical Trials; Massachusetts; Remote; USD 90,000 - 120,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate for a home-based role on the East Coast. You will monitor investigative sites, ensure protocol adherence and data quality, and collaborate with global teams to support study milestones.

The position requires 5+ years as a regional traveling CRA with oncology monitoring experience and willingness to travel regionally. Join a global CRO that values patient safety and rigorous study conduct.

Qualifications

• Bachelor's Degree or Nursing Degree with 5+ years as a regional traveling Clinical Research Associate.
• Experience monitoring Oncology clinical trials (gastric cancer experience preferred).
• Requires regional travel; travel 8–10 days per month.

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

Travel required

Oncology trials

Education

Bachelor's or Nursing degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate for a home-based role on the East Coast. You will monitor investigative sites, ensure protocol adherence and data quality, and collaborate with global teams to support study milestones.

The position requires 5+ years as a regional traveling CRA with oncology monitoring experience and willingness to travel regionally. Join a global CRO that values patient safety and rigorous study conduct.