Senior Clinical Research Associate - Oncology (Southeast/MidAtlantic)

Worldwide Clinical Trials • Carolina, NC

1d • Remote

About The Position

Worldwide Clinical Trials is hiring a Senior Clinical Research Associate to support oncology clinical studies at investigative sites across the Southeast and Mid-Atlantic. This is a home-based role, and candidates must reside within the territory. The role involves regional travel to investigative sites approximately 8–10 days per month, with occasional travel to other locations as needed.

The Senior CRA oversees clinical study activities from site qualification through closeout, supporting quality, patient safety, regulatory compliance, reliable data, and effective site performance. The role partners with investigative sites, study teams, and sponsors, providing monitoring, site management, leadership, guidance, and oversight throughout the clinical trial lifecycle.

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.
• Reside within the Southeast or Mid-Atlantic territory.

Nice To Haves

• Experience in full-service monitoring.

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, study initiation, interim monitoring, and closeout visits.
• 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 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