Senior Clinical Research Associate - Oncology (US, East Coast)

Worldwide Clinical Trials • New York, MA

1d • $97,000 - $193,000 • Remote

About The Position

Worldwide Clinical Trials is hiring a home-based Senior Clinical Research Associate to support oncology clinical studies at investigative sites across the East Coast of the United States. The role requires residence within the territory and travel to investigative sites approximately 8–10 days per month, primarily regionally, with occasional travel elsewhere as needed.

The Senior CRA oversees clinical research activities from site qualification through closeout, supporting patient safety, data quality, protocol adherence, and regulatory compliance. The role partners with investigative sites, sponsors, study teams, and global colleagues to support successful study execution and site performance.

Requirements

• Bachelor's degree or nursing degree.
• At least 5 years of experience as a regional, traveling Clinical Research Associate.
• Experience monitoring oncology clinical trials.
• Ability to travel within the specified region, approximately 8–10 days per month.
• Strong knowledge of clinical trial processes, site management, and regulatory requirements.

Nice To Haves

• Gastric cancer clinical trial experience is preferred.
• Experience in full-service monitoring is preferred.

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 collecting regulatory documentation and supporting contract and budget processes.
• Conduct 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 support data quality, participant safety, and overall study success.
• Support site closeout activities and ensure study requirements are completed at the conclusion of the trial.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior