Senior CRA II: Global Site Monitoring & Study Excellence

Parexel; Washington (District of Columbia); On-site; USD 95,000 - 130,000; Full time

Job summary

Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to oversee investigator sites, ensure patient safety, and monitor study progress in accordance with GCP and sponsor standards.

The role requires close collaboration with the Site Care Partner and study team to drive site performance from activation through database lock. Ideal candidates have a life sciences background, 2+ years of monitoring experience, and the ability to travel extensively.

Qualifications

• Minimum 2 years relevant experience in clinical research site monitoring.
• Fluent in English and in the native language(s) of the country worked in.
• Ability to travel 60-80%.
• Valid driver’s license and passport required.

Responsibilities

• Site management and monitoring to ensure patient safety and study quality.
• Manage investigator site relationships to ensure enrollment and data delivery.
• Prepare and handle site activation, monitoring visits, and close-out activities.
• Coordinate with SCP and study team to resolve protocol-related issues.

Education

Bachelor’s degree in life sciences

Job description

Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to oversee investigator sites, ensure patient safety, and monitor study progress in accordance with GCP and sponsor standards.

The role requires close collaboration with the Site Care Partner and study team to drive site performance from activation through database lock. Ideal candidates have a life sciences background, 2+ years of monitoring experience, and the ability to travel extensively.