Oncology CRA | Global Site Management & Monitoring

Parexel; Richmond (VA); On-site; 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 study phases. You will oversee site relationships, ensure adherence to GCP/ICH, and manage regulatory documentation. The role requires strong communication, data integrity, and the ability to travel up to 75% of the time.

Oncology experience is preferred, multi-specialty encouraged. US locations are available with West and Central regions favored.

Qualifications

• 2 years of site monitoring experience
• Bachelor's degree preferred

Responsibilities

• Act as the primary site contact and site manager throughout all phases of a clinical research study
• Ensure data generated at site is complete, accurate and unbiased
• Collect, review, and monitor regulatory documentation for study start-up, maintenance and close-out
• Travel domestically and internationally approximately 65%-75% of working time

Skills

Site management

Monitoring

GCP/ICH

Communication

Data analysis

Education

Bachelor's degree

Job description

Parexel is seeking a Clinical Research Associate to act as the primary site contact and site manager across all study phases. You will oversee site relationships, ensure adherence to GCP/ICH, and manage regulatory documentation. The role requires strong communication, data integrity, and the ability to travel up to 75% of the time.

Oncology experience is preferred, multi-specialty encouraged. US locations are available with West and Central regions favored.