Remote Clinical Research Associate II – Site Management

Parexel; Montpelier (VT); Remote; USD 60,000 - 90,000; Full time

Job summary

Parexel is seeking a Clinical Research Associate to act as primary site contact and site manager across all phases of a clinical study. The role emphasizes site relationships, monitoring visits, and regulatory documentation to ensure data integrity and patient safety.

The candidate should have 2+ years of direct site monitoring experience, familiarity with ICH-GCP and sponsor SOPs, and a Bachelor’s degree preferred. This position supports remote work with focus on US sites, including Vermont.

Qualifications

• 2+ years of direct site monitoring experience in bio/pharma/CRO.
• Experience working within ICH-GCP guidelines and sponsor SOPs.
• Strong communication and problem-solving abilities.

Responsibilities

• Manage and monitor clinical trial sites across multiple protocols.
• Maintain regulatory documentation and trial master file accuracy.
• Ensure data integrity and subject safety through site visits and remote monitoring.
• Collaborate with sponsors, investigators and site staff to resolve issues.

Skills

Site management

ICH-GCP compliance

Clinical monitoring

Data integrity

Education

Bachelor's degree preferred

Tools

MS Office

Clinical IT applications

Job description

Parexel is seeking a Clinical Research Associate to act as primary site contact and site manager across all phases of a clinical study. The role emphasizes site relationships, monitoring visits, and regulatory documentation to ensure data integrity and patient safety.

The candidate should have 2+ years of direct site monitoring experience, familiarity with ICH-GCP and sponsor SOPs, and a Bachelor’s degree preferred. This position supports remote work with focus on US sites, including Vermont.