Senior CRA - Oncology (Remote, East Coast Travel)

Worldwide Clinical Trials Holdings, Inc.

Massachusetts

Hybrid

USD 97,000 - 193,000

Full time

14 days+

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Benefits offered by this job

Competitive benefits package

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to ensure studies meet high standards of quality, patient safety, and regulatory compliance. You will serve as a trusted partner to investigative sites, study teams, and sponsors, leading monitoring activities from site qualification through closeout.

This home-based role supports East Coast sites with travel about 8–10 days per month. Ideal candidates have 5+ years as a regional CRA and Oncology trial experience.

Qualifications

  • 5+ years as a regional, traveling Clinical Research Associate
  • Experience monitoring Oncology trials (gastric cancer experience preferred)
  • Willingness to travel 8–10 days per month within the East Coast region
  • Strong knowledge of GCP and regulatory requirements

Responsibilities

  • Manage clinical research activities at investigative sites participating in Worldwide studies.
  • Identify and assess potential research sites to support study execution.
  • Coordinate study start-up activities and support contract/budget processes.
  • Conduct monitoring visits (PSSVs, SIVs, IMVs, COVs).
  • Train site personnel on protocol requirements and safety reporting.
  • Monitor site performance and provide ongoing support during maintenance.
  • Ensure informed consent, safety reporting and regulatory compliance.
  • Partner with sites and study teams to drive data quality and participant safety.

Skills

Senior CRA experience
Oncology monitoring
Site management
Regulatory compliance
Travel readiness

Education

Bachelor’s Degree or Nursing Degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to ensure studies meet high standards of quality, patient safety, and regulatory compliance. You will serve as a trusted partner to investigative sites, study teams, and sponsors, leading monitoring activities from site qualification through closeout.

This home-based role supports East Coast sites with travel about 8–10 days per month. Ideal candidates have 5+ years as a regional CRA and Oncology trial experience.

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