Remote CRA II: Site Monitoring & Trial Oversight

Parexel; Montgomery (AL); Remote; USD 65,000 - 95,000; Full time

Job summary

Parexel is seeking a Clinical Research Associate (CRA) to manage investigator sites, monitor trials for quality and patient safety, and ensure regulatory compliance across the study lifecycle. You will coordinate with Site Care Partners and study teams to optimize site performance and enrollment.

The role requires travel, strong knowledge of GCP/ICH, and the ability to operate in a dynamic environment while maintaining sponsor standards and timelines.

Qualifications

• Bachelor’s degree in life sciences or related field.
• Minimum 2 years in clinical trial monitoring or site management preferred.
• Fluency in English and local country language where the role is based.

Responsibilities

• Monitor investigator sites to ensure compliance with GCP and SMP.
• Serve as primary contact for sites and coordinate with SCP and study team.
• Attend site activations, monitoring visits, and close-out activities.
• Ensure timely submission of TMF documents and site reports.
• Support recruitment and site performance through training and coaching.

Skills

Clinical trial methodologies

ICH/GCP

FDA regulations

Local regulations

English fluency

Travel availability

Driver’s license & passport

Education

Bachelor's in life sciences

Job description

Parexel is seeking a Clinical Research Associate (CRA) to manage investigator sites, monitor trials for quality and patient safety, and ensure regulatory compliance across the study lifecycle. You will coordinate with Site Care Partners and study teams to optimize site performance and enrollment.

The role requires travel, strong knowledge of GCP/ICH, and the ability to operate in a dynamic environment while maintaining sponsor standards and timelines.