Senior CRA - Remote Oncology Trials Lead (Regional Travel)

Worldwide Clinical Trials Holdings, Inc.; North Carolina; Teletrabalho; USD 97 000 - 193 000; Tempo integral

Resumo da oferta

Worldwide Clinical Trials Holdings, Inc. is seeking a Senior Clinical Research Associate for a home-based role supporting Southeast or Mid-Atlantic US sites.

The position requires 5+ years as a regional CRA with oncology trial monitoring experience and travel of 8–10 days per month. You will lead monitoring activities, ensure regulatory compliance, and partner with sponsors and investigative sites to drive data quality and study success.

Qualificações

• Bachelor's Degree or a Nursing Degree required.
• 5+ years as a regional, traveling CRA.
• Experience monitoring Oncology clinical trials.
• Willingness to travel within the specified region; some visits may be remote.
• Experience in full-service monitoring is preferred.

Responsabilidades

• 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 regulatory documentation and contract/budget support.
• Conduct monitoring visits: PSSVs, SIVs, IMVs, COVs.
• Train site personnel on protocol requirements, data collection, and safety reporting.
• Monitor site performance and provide ongoing support during study maintenance.
• Ensure informed consent, safety reporting, and regulatory compliance.
• Collaborate with sites and study teams to drive data quality and participant safety.
• Support site closeout activities and ensure study requirements are completed.

Conhecimentos

Oncology trials experience

Travel within region

Full-service monitoring

Site management

Formação académica

Bachelor's or Nursing degree

Descrição da oferta de emprego

Worldwide Clinical Trials Holdings, Inc. is seeking a Senior Clinical Research Associate for a home-based role supporting Southeast or Mid-Atlantic US sites.

The position requires 5+ years as a regional CRA with oncology trial monitoring experience and travel of 8–10 days per month. You will lead monitoring activities, ensure regulatory compliance, and partner with sponsors and investigative sites to drive data quality and study success.