CRA II: Field Monitoring & Site Management

Parexel; Phoenix (AZ); On-site; USD 70,000 - 110,000; Full time

Job summary

Parexel is seeking a Clinical Research Associate to manage investigator sites across assigned trials in the United States. You will monitor study conduct, ensure patient safety, quality, and regulatory compliance while maintaining strong site relationships and supporting enrollment and data integrity.

Travel will be required to active sites. Primary responsibilities include coordinating with the Site Care Partner and study team, performing monitoring activities, and ensuring timely, accurate

Qualifications

• Bachelor’s degree in life sciences or nursing/pharmacy/medical background.
• Minimum 2 years monitoring experience in clinical research.

Responsibilities

• Ensure proper conduct of clinical trials per SMP, laws, GCP and Sponsor standards to meet timelines and quality.
• Manage operational aspects of site activation through database lock.
• Serve as primary contact for investigator sites; collaborate with SCP for site delivery quality.
• Interface with study team, vendors, and sites to ensure smooth information flow.
• Perform investigator site development, coaching and training to ensure protocol compliance and patient safety.
• Attend investigator meetings and provide enrollment support; coordinate recruitment initiatives at site level.
• Conduct onsite or remote monitoring as per SMP; ensure appropriate documentation and compliance.
• Monitor site adverse events and SAEs; coordinate with Drug Safety for resolution.
• Submit required TMF documentation, site reports, deviations, recruitment metrics and other updates.

Skills

Clinical trial knowledge

GCP/ICH compliance

English fluency

Travel readiness

Driver's license & passport

Education

Bachelor's degree in life sciences

Job description

Parexel is seeking a Clinical Research Associate to manage investigator sites across assigned trials in the United States. You will monitor study conduct, ensure patient safety, quality, and regulatory compliance while maintaining strong site relationships and supporting enrollment and data integrity.

Travel will be required to active sites. Primary responsibilities include coordinating with the Site Care Partner and study team, performing monitoring activities, and ensuring timely, accurate