Clinical Research Associate Jobs

About The Position

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.