Clinical Research Associate II – Remote (West US)

Parexel; Jackson (MS); Remote; USD 55,000 - 75,000; Full time

Job summary

Parexel is seeking a Clinical Research Associate to manage study sites and serve as the primary contact across all trial phases. The role emphasizes site relationships, monitoring, and adherence to ICH-GCP, SOPs, and regulatory requirements.

The candidate will coordinate with sponsor teams, perform remote and on-site visits, and maintain trial documentation in CTMS/eTMF while ensuring patient safety and data integrity.

Qualifications

• Bachelor’s degree preferred with strong science background.
• Minimum 2 years of direct site monitoring experience.
• Fluent in local languages and English.

Responsibilities

• Develops strong site relationships through all trial phases.
• Performs site monitoring in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations.
• Collects regulatory documentation for study start-up, maintenance and close-out.
• Communicates with investigators and site staff on protocol conduct and regulatory documentation.
• Maintains documentation in CTMS/eTMF and other systems.

Skills

Site management

Monitoring

Communication

IT skills

Independent judgement

Education

Bachelor’s degree

Job description

Parexel is seeking a Clinical Research Associate to manage study sites and serve as the primary contact across all trial phases. The role emphasizes site relationships, monitoring, and adherence to ICH-GCP, SOPs, and regulatory requirements.

The candidate will coordinate with sponsor teams, perform remote and on-site visits, and maintain trial documentation in CTMS/eTMF while ensuring patient safety and data integrity.