Remote CRA II – West Coast Site Monitor

Parexel; Phoenix (AZ); Remote; USD 65,000 - 90,000; 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 emphasizes building strong site relationships and ensuring compliant, timely data collection and regulatory documentation.

The CRA will perform monitoring activities both remotely and onsite, participate in site selection processes, and maintain trial records in the TMF and other systems.

Qualifications

• Minimum 2 years of direct site monitoring experience in bio/pharma/CRO.
• Bachelor’s degree preferred with a strong emphasis in science and /or biology.

Responsibilities

• Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.
• Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated Documents.
• Gains an in-depth understanding of the study protocol and related procedures.
• Coordinates and manages tasks in collaboration with sponsor roles to achieve Site Ready.
• Participates and provides inputs on site selection and validation activities.
• Performs remote and on-site monitoring & oversight activities to ensure data integrity and subject safety.
• Collects, reviews, and monitors required regulatory documentation for study start-up, maintenance and close-out.
• Communicates with Investigators and site staff on protocol conduct, recruitment, retention, regulatory documentation, site audits/inspections and overall site performance.

Skills

English proficiency

Clinical trials knowledge

Site management

Monitoring experience

Data analysis

MS Office

IT applications

Education

Bachelor’s degree in science

Tools

eTMF systems

Clinical IT applications

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 emphasizes building strong site relationships and ensuring compliant, timely data collection and regulatory documentation.

The CRA will perform monitoring activities both remotely and onsite, participate in site selection processes, and maintain trial records in the TMF and other systems.