Senior CRA – Remote Site Monitoring & Oversight

Parexel; Olympia (WA); On-site; USD 90,000 - 130,000; Full time

Job summary

Parexel FSP in the US is seeking a Senior Clinical Research Associate (Sr CRA) to lead site management, monitoring, and close-out of assigned trials, ensuring patient safety and data quality in accordance with GCP and client standards. The role emphasizes proactive site partnerships, issue resolution, and robust documentation across TMF and study milestones.

The Sr CRA works with the Site Care Partner and study team to support site activation, enrollment, and risk management, and travels

Qualifications

• Extensive knowledge of clinical trial methodologies and GCP.
• Strong understanding of regulatory requirements (FDA, ICH/GCP).
• Experience in site monitoring and management activities.

Responsibilities

• Oversee site management and monitoring to ensure patient safety and data quality.
• Coordinate with SCP and study team for activation, enrollment and close-out.
• Ensure timely trial deliverables and accurate documentation (TMF).
• Identify and mitigate site-level risks and CAPA development.
• Support enrollment strategies and site communication during studies.

Skills

Clinical monitoring

GCP knowledge

Regulatory compliance

Site management

Communication

Education

Bachelor's degree in life sciences or allied field

Job description

Parexel FSP in the US is seeking a Senior Clinical Research Associate (Sr CRA) to lead site management, monitoring, and close-out of assigned trials, ensuring patient safety and data quality in accordance with GCP and client standards. The role emphasizes proactive site partnerships, issue resolution, and robust documentation across TMF and study milestones.

The Sr CRA works with the Site Care Partner and study team to support site activation, enrollment, and risk management, and travels