Remote Clinical Research Associate | Senior CRA

Parexel; Springfield (IL); On-site; USD 70,000 - 110,000; Full time

Job summary

Parexel is seeking a Clinical Research Associate (CRA) / Sr CRA for sites in the United States, including Springfield, IL. The role covers initiation, monitoring, and close-out of sites, with an emphasis on quality, regulatory compliance, and timely data delivery.

You will train investigators, manage site relationships, and ensure CTMS data integrity while coordinating with local study teams and LSAD to meet study commitments.

Qualifications

• Excellent knowledge of ICH-GCP and related clinical regulations.
• Ability to manage site relationships and monitor study progress.
• Fluent written and spoken English; local language skills helpful.

Responsibilities

• Oversee site selection, initiation, monitoring and closure per plan.
• Train and support Investigators and site staff on study procedures.
• Ensure regulatory submissions and documentation are up to date.
• Maintain CTMS data, manage study drug accountability and supply.
• Prepare monitoring visit reports and track site performance.

Skills

Attention to detail

Written English

Communication

Collaboration

Negotiation

Education

Bachelor’s degree in life sciences or related

Job description

Parexel is seeking a Clinical Research Associate (CRA) / Sr CRA for sites in the United States, including Springfield, IL. The role covers initiation, monitoring, and close-out of sites, with an emphasis on quality, regulatory compliance, and timely data delivery.

You will train investigators, manage site relationships, and ensure CTMS data integrity while coordinating with local study teams and LSAD to meet study commitments.