Remote CRA: Oncology Trials & Site Oversight

Parexel; Lincoln (NE); On-site; USD 65,000 - 95,000; Full time

Job summary

Parexel is hiring a Clinical Research Associate in the United States, with a focus on site management across multiple sites and trial phases. The role emphasizes ensuring data integrity, regulatory compliance, and site performance while working in a fast-paced, matrix environment.

Preferred candidates have oncology experience and are willing to travel domestically and internationally about 65–75% of the time.

Qualifications

• Minimum 2 years of direct site monitoring experience in bio/pharma/CRO.
• Solid knowledge of ICH-GCP and country regulations.
• Bachelor’s degree in science or related field preferred.

Responsibilities

• Act as the primary site contact and site manager throughout all phases of a clinical trial.
• Coordinate and perform site monitoring activities in compliance with ICH-GCP, Sponsor SOPs, and regulatory requirements.
• Maintain study documentation in the TMF/eTMF systems and ensure timely, accurate reports.

Skills

Site management

Monitoring visits

ICH-GCP knowledge

Regulatory documentation

Data review

Communication skills

Travel readiness

Team mentoring

Education

Bachelor’s degree

Job description

Parexel is hiring a Clinical Research Associate in the United States, with a focus on site management across multiple sites and trial phases. The role emphasizes ensuring data integrity, regulatory compliance, and site performance while working in a fast-paced, matrix environment.

Preferred candidates have oncology experience and are willing to travel domestically and internationally about 65–75% of the time.