Remote Clinical Research Associate – Oncology Trials

Parexel; Austin (TX); Remote; USD 70,000 - 110,000; Full time

Job summary

Parexel is seeking a Clinical Research Associate to act as the primary site contact and site manager across all phases of a clinical trial. You will develop strong site relationships, ensure regulatory compliance, and coordinate with sponsor roles to achieve site readiness.

Responsibilities include monitoring visits, regulatory documentation, and communicating issues related to protocol conduct, recruitment, and site performance. Travel up to 65–75% domestically and internationally is required.

Qualifications

• Experience in site management/monitoring for clinical trials.
• Familiarity with ICH-GCPs, regulatory documentation, and study start-up/close-out processes.
• Ability to manage multiple sites and communicate with investigators and staff.

Responsibilities

• Act as primary site contact and site manager across all study phases.
• Coordinate site readiness and maintenance, ensure data is accurate and compliant.
• Conduct site visits: initiation, monitoring, closeout; generate reports.

Skills

Site management

Clinical monitoring

ICH-GCP knowledge

Regulatory compliance

Data interpretation

Communication

Travel readiness

Problem solving

Education

Bachelor’s degree preferred

Job description

Parexel is seeking a Clinical Research Associate to act as the primary site contact and site manager across all phases of a clinical trial. You will develop strong site relationships, ensure regulatory compliance, and coordinate with sponsor roles to achieve site readiness.

Responsibilities include monitoring visits, regulatory documentation, and communicating issues related to protocol conduct, recruitment, and site performance. Travel up to 65–75% domestically and internationally is required.