Note: The job is a remote job and is open to candidates in USA. Worldwide Clinical Trials is hiring a Senior Clinical Research Associate to manage and monitor oncology clinical studies at investigative sites across the East Coast. The role supports study execution from site selection and start-up through closeout, ensuring protocol adherence, regulatory compliance, data quality, and participant safety.

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: Pre-Site Selection Visits (PSSVs), Study Initiation Visits (SIVs),Interim Monitoring Visits (IMVs) and Closeout Visits (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

• Bachelor's Degree or a Nursing Degree, along with 5+ years as a regional, traveling Clinical Research Associate
• Required experience monitoring Oncology clinical trials
• Strong knowledge of clinical trial processes, site management, and regulatory requirements
• Experience in full-service monitoring preferred

Benefits

• Home-based role supporting sites across the East Coast; candidates must reside within the territory and travel to investigative sites approximately 8–10 days per month.

Company Overview

Company H1B Sponsorship