Remote Clinical Research Associate II - Site Monitoring

Parexel; Boise (ID); 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. You will build strong site relationships, monitor compliance, and ensure data integrity and patient safety.

Responsibilities include site visits, regulatory documentation, communication with investigators, and collaboration with sponsor teams to drive trial readiness while adhering to ICH-GCP, local laws, and Parexel standards.

Qualifications

• Minimum 2 years of direct site monitoring experience in bio/pharma/CRO.
• Bachelor's degree preferred with science emphasis.
• Strong knowledge of ICH-GCP and regulatory requirements.

Responsibilities

• Develops strong site relationships and ensures continuity of site relationships.
• Performs site monitoring in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations.
• Gains understanding of study protocol and procedures.
• Coordinates with sponsor roles to achieve Site Ready.
• Performs remote and on-site monitoring to ensure data accuracy and patient safety.
• Maintains documentation in CTMS and eTMF.

Skills

Site management

GCP/ICH

Data monitoring

Documentation

Communication

MS Office

Education

Bachelor's degree

Tools

Clinical IT tools

eTMF

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. You will build strong site relationships, monitor compliance, and ensure data integrity and patient safety.

Responsibilities include site visits, regulatory documentation, communication with investigators, and collaboration with sponsor teams to drive trial readiness while adhering to ICH-GCP, local laws, and Parexel standards.