Senior Clinical Research Associate (Remote)

Parexel; Oklahoma City (OK); On-site; USD 65,000 - 90,000; Full time

Job summary

Parexel in the United States is seeking a Clinical Research Associate to oversee site management, monitoring, and close-out of investigator sites to ensure patient safety and quality study execution.

You will act as primary contact for sites, support enrollment efforts, and collaborate with the Site Care Partner to address protocol and operational risks.

This role requires 2+ years of monitoring experience, travel up to 80%, and a strong knowledge of GCP and regulatory standards.

Qualifications

• Bachelor’s degree in life sciences or related field.
• Minimum 2 years monitoring experience in clinical research.
• Fluent English and local language(s) as required.
• Willingness to travel 60–80%.
• Valid driver’s license and passport required.

Responsibilities

• Monitor investigator sites to ensure patient safety and data integrity.
• Manage site activation, monitoring, and close-out per SMP and SOPs.
• Coordinate with Site Care Partner and study team to optimize site performance.
• Prepare site reports, documents, and study progress metrics.
• Support enrollment and recruitment activities at sites.
• Ensure regulatory compliance and escalate issues as needed.

Skills

Clinical trial knowledge

Monitoring experience

Fluent English

Travel readiness

Driver's license & passport

Education

Bachelor’s degree in life sciences

Job description

Parexel in the United States is seeking a Clinical Research Associate to oversee site management, monitoring, and close-out of investigator sites to ensure patient safety and quality study execution.

You will act as primary contact for sites, support enrollment efforts, and collaborate with the Site Care Partner to address protocol and operational risks.

This role requires 2+ years of monitoring experience, travel up to 80%, and a strong knowledge of GCP and regulatory standards.