Remote CRA II, West US — Site Management & Monitoring

Parexel; Denver (CO); Remote; USD 70,000 - 100,000; Full time

Job summary

Parexel is seeking a Clinical Research Associate to serve as the primary site contact and site manager across all phases of a clinical study. The role requires building strong site relationships, monitoring for data integrity and patient safety, and ensuring regulatory compliance.

The CRA will coordinate with sponsor teams, conduct visits (on-site and remote), and maintain essential documentation in the TMF. Strong communication and independent problem solving are essential for success.

Qualifications

• Minimum 2 years of direct site monitoring experience in bio/pharma/CRO.
• Strong knowledge of ICH-GCP and regulatory documentation.
• Excellent communication and cross-functional collaboration skills.
• Proficient with clinical trial management systems and MS Office.

Responsibilities

• Develops strong site relationships across all trial phases.
• Performs monitoring visits and ensures data accuracy and safety.
• Manages regulatory documentation for start-up, maintenance and close-out.
• Communicates findings to Investigators and sponsor team.
• Escalates site performance issues per escalation paths.

Skills

Site relationship management

ICh-GCP knowledge

Regulatory documentation

Communication skills

Data analysis

MS Office

Independent problem solving

Multitasking

Cross-functional collaboration

Education

Bachelor’s degree in science or related field

Tools

MS Office

Job description

Parexel is seeking a Clinical Research Associate to serve as the primary site contact and site manager across all phases of a clinical study. The role requires building strong site relationships, monitoring for data integrity and patient safety, and ensuring regulatory compliance.

The CRA will coordinate with sponsor teams, conduct visits (on-site and remote), and maintain essential documentation in the TMF. Strong communication and independent problem solving are essential for success.